Cyclopentenes ketones

Diketones are readily transformed to cycHc derivatives, such as cyclopentanones and furans. In this manner, the fragrance dihydrojasmone (3-meth5l-2-pentyl-2-cyclopenten-l-one) is prepared by the base-catalyzed aldol condensation of 2,5-undecanedione. 2,5-Undecanedione is itself prepared from heptanal and methyl vinyl ketone in the presence of thiazoHum salts (329). i7j -Jasmone can be similarly prepared (330,331). 

Many cycHc ketones occur in natural oils. Jasmone [488-10-8] (3-meth5l-2-(2-pentyl)-2-cyclopenten-l-one) (4) is an odoriferous component of the oil obtained from jasmine flowers. /-Menthone [14073-97-3] (5) is the most frequently occurring of four optically active isomers, and is a colorless Hquid with a minty odor obtained from Mentha species of plants. Muscone [541-91-3] (6) and civetone [542-46-1] (7) are expensive animal products. 

Chemically, wood tar is a complex mixture that contains at least 200 individual compounds, among which the foUowing have been isolated (1) 2-methoxyphenol, 2-methoxy-4-ethylphenol, 5-meth5i-2-methoxyphenol, 2,6-x5ienol, butyric acid, crotonic acid, 1-hydroxy-2-propanone, butyrolactone, 2-methyl-3-hydroxy-4JT-pyran-4-one, 2-methyl-2-propenal, methyl ethyl ketone, methyl isopropyl ketone, methyl furyl ketone, and 2-hydroxy-3-methyl-2-cyclopenten-l-one. 

Since 1,5-enediones are usually obtained via pyrylium salts, syntheses of the type found in Section B, 2, a have a rather theroetical interest, save for a few special syntheses. There exist several direct syntheses of l,5-enediones, e.g., from j8-chlorovinyl ketones and j8-diketones or j8-keto esters special pathways to 1,5-enediones have also been described, namely, oxidation with lead tetraacetate or with periodic acid of cyclopentene-l,2-diols. ... 

In a 200-ml three-necked flask fitted with a dropping funnel (drying tube) is placed a solution of 13.4 g (0.12 mole) of 1-octene in 35 ml of THF. The flask is flushed with nitrogen and 3.7 ml of a 0.5 M solution of diborane (0.012 mole of hydride) in THF is added to carry out the hydroboration. (See Chapter 4, Section I regarding preparation of diborane in THF.) After 1 hour, 1.8 ml (0.1 mole) of water is added, followed by 4.4 g (0.06 mole) of methyl vinyl ketone, and the mixture is stirred for 1 hour at room temperature. The solvent is removed, and the residue is dissolved in ether, dried, and distilled. 2-Dodecanone has bp 119710 mm, 24571 atm. (The product contains 15 % of 5-methyl-2-undecane.) The reaction sequence can be applied successfully to a variety of olefins including cyclopentene, cyclohexene, and norbornene. 

An interesting strategy for the diastereoselective synthesis of five-membered carbocycles was achieved by the reaction of alkenylcarbene complexes and lithium enolates derived from simple methyl ketones [79]. The use of more or less coordinating solvents (THF or Et20) or the presence of cosolvents such as PMDTA allows the selective synthesis of one or the other diastereoisomer of the final cyclopentene derivative (Scheme 32). 

Die Reaktion lauft beim 2,5-Dibrom-cyclopentanon auch ohne Saure-Zusatz ab (43% d. Th. Cyclopentanon)-, in Gcgenwart von Saure erhalt man die x/l-ungesattigten Ketone. So erhalt man z.B. aus 4-Brom-3-oxo-2,4-dimethyl-cyclopenten 32% d. Th. 3-Oxo-2,4-dimethyl-cyclopenten1 ... 

The presence of the catalyst can also favor multiple Diels-Alder reactions of cycloalkenones. Two typical examples are reported in Schemes 3.6 and 3.7. When (E)-l-methoxy-1,3-butadiene (14) interacted with 2-cyclohexenone in the presence of Yb(fod)3 catalyst, a multiple Diels-Alder reaction occurred [21] and afforded a 1 1.5 mixture of the two tricyclic ketones 15 and 16 (Scheme 3.6). The sequence of events leading to the products includes the elimination of methanol from the primary cycloadduct to afford a bicyclic dienone that underwent a second cycloaddition. Similarly, 4-acetoxy-2-cyclopenten-l-one (17) (Scheme 3.7) has been shown to behave as a conjunctive reagent for a one-pot multiple Diels-Alder reaction with a variety of dienes under AICI3 catalysis, providing a mild and convenient methodology to synthesize hydrofluorenones [22]. The role of the Lewis acid is crucial to facilitate the elimination of acetic acid from the cycloadducts. The results of the reaction of 17 with diene... 

NHC-promoted enolate formation from an enal, followed by a desymmetrising aldol event to generate P-lactones and loss of CO, has been exploited by Scheidt and co-workers to generate functionalised cyclopentenes 240 in high ee from enal substrates 238 (Scheme 12.52) [94]. Interestingly, the use of alkyl ketones in this reaction manifold allows the isolation of the p-lactone intermediates with acyclic diketones, P-lactones 239 are formed with the R group anti- to the tertiary alkox-ide, while with cyclic diketones the P-lactone products have the R group with a syn relationship to the alkoxide [95]. 

In order to establish the correct absolute stereochemistry in cyclopentanoid 123 (Scheme 10.11), a chirality transfer strategy was employed with aldehyde 117, obtained from (S)-(-)-limonene (Scheme 10.11). A modified procedure for the conversion of (S)-(-)-limonene to cyclopentene 117 (58 % from limonene) was used [58], and aldehyde 117 was reduced with diisobutylaluminium hydride (DIBAL) (quant.) and alkylated to provide tributylstannane ether 118. This compound underwent a Still-Wittig rearrangement upon treatment with n-butyl lithium (n-BuLi) to yield 119 (75 %, two steps) [59]. The extent to which the chirality transfer was successful was deemed quantitative on the basis of conversion of alcohol 119 to its (+)-(9-methyI mande I ic acid ester and subsequent analysis of optical purity. The ozonolysis (70 %) of 119, protection of the free alcohol as the silyl ether (85 %), and reduction of the ketone with DIBAL (quant.) gave alcohol 120. Elimination of the alcohol in 120 with phosphorus oxychloride-pyridine... 

The photoindueed 1,7-cycloaddition of carbon monoxide across the divinyl-cyclopropane derivative 32 yields the two cyclic dienyl ketones 34, via the ferracyclononadiene intermediate 33 [18]. (Scheme 11) cyclopentene rearrangement. The dienylcyclopropane 35 is capable of forming the complex 36, followed by ring enlargement to 37 [19]. 1,1-Dicyclopropylethylene 29 is also converted to the 1-cyclopropyl-1-cyclopentene 38. The additional functionality of vinylcyclopropanes is necessary to serve as a 7t-donor... 

The 0/7/fo-alkylation of aromatic ketones with olefins can also be achieved by using the rhodium bis-olefin complex [C5Me5Rh(C2H3SiMe3)2] 2, as shown in Equation (9).7 This reaction is applied to a series of olefins (allyltrimethyl-silane, 1-pentene, norbornene, 2,2 -dimethyl-3-butene, cyclopentene, and vinyl ethyl ether) and aromatic ketones (benzophenone, 4,4 -dimethoxybenzophenone, 3,3 -bis(trifluoromethyl)benzophenone, dibenzosuberone, acetophenone, />-chloroacetophenone, and />-(trifluoromethyl)acetophenone). 

The results of the olefin oxidation catalyzed by 19, 57, and 59-62 are summarized in Tables VI-VIII. Table VI shows that linear terminal olefins are selectively oxidized to 2-ketones, whereas cyclic olefins (cyclohexene and norbomene) are selectively oxidized to epoxides. Cyclopentene shows exceptional behavior, it is oxidized exclusively to cyclopentanone without any production of epoxypentane. This exception would be brought about by the more restrained and planar pen-tene ring, compared with other larger cyclic nonplanar olefins in Table VI, but the exact reason is not yet known. Linear inner olefin, 2-octene, is oxidized to both 2- and 3-octanones. 2-Methyl-2-butene is oxidized to 3-methyl-2-butanone, while ethyl vinyl ether is oxidized to acetaldehyde and ethyl alcohol. These products were identified by NMR, but could not be quantitatively determined because of the existence of overlapping small peaks in the GC chart. The last reaction corresponds to oxidative hydrolysis of ethyl vinyl ether. Those olefins having bulky (a-methylstyrene, j8-methylstyrene, and allylbenzene) or electon-withdrawing substituents (1-bromo-l-propene, 1-chloro-l-pro-pene, fumalonitrile, acrylonitrile, and methylacrylate) are not oxidized. 

A regioselective [3 + 2]-cycloaddition approach to substituted 5-membered carbo-cycles was made available by the use of allenylsilanes [188]. The reaction involves regioselective attack of an unsaturated ketone by (trimethylsilyl)allene at the 3-position. The resulting vinyl cation undergoes a 1,2-silyl migration. The isomeric vinyl cation is intercepted intramolecularly by the titanium enolate to produce a highly substituted (trimethylsilyl)cyclopentene derivative. 

Recordings from Staphylininae [115] include 3-methylbutanal, the corresponding alcohol, and its acetate, various ketones such as 4-methyl-3-hexanone, 4-methyl-3-heptanone, 5-methyl-3-hexanone (and the corresponding alcohol), 2-heptanone, 6-methyl-2-heptanone, 6-methyl-5-hepten-2-one as well as methyl-cyclopentene and methylfuran. In addition, the secretions of Ontholestes murinus contain the spiroacetals (2S,6R,8S)-2,8-dimethyl-l,7-dioxaspiro[5,5]-... 

In fluorosulfonic acid the anodic oxidation of cyclohexane in the presence of different acids (RCO2H) leads to a single product with a rearranged carbon skeleton, a 1-acyl-2-methyl-1-cyclopentene (1) in 50 to 60% yield (Eq. 2) [7, 8]. Also other alkanes have been converted at a smooth platinum anode into the corresponding a,-unsaturated ketones in 42 to 71% yield (Table 1) [8, 9]. Product formation is proposed to occur by oxidation of the hydrocarbon to a carbocation (Eq. 1 and Scheme 1) that rearranges and gets deprotonated to an alkene, which subsequently reacts with an acylium cation from the carboxylic acid to afford the a-unsaturated ketone (1) (Eq. 2) [8-10]. In the absence of acetic acid, for example, in fluorosulfonic acid/sodium... 

Cyclohexene, see Cyclohexene Cyclohexyl alcohol, see Cyclohexanol Cyclohexyl ketone, see Cyclohexanone Cyclohexylmethane, see Methylcyclohexane Cyclopenta-1,3-diene, see Cyclopentadiene 1,3-Cyclopentadiene, see Cyclopentadiene Cyclopentamethylene, see Cyclopentane Cyclopenta[(/,e]naphthalene. see Acenaphthylene Cyclopenten, see Cyclopentene Cyclopentenyl, see Cyclopentene... 

Hudlicky saw in 651 an occasion to apply a-diazo ketone cyclization methodology With cyclopentene aldehyde 660 as the starting point, dienyl carboxyhc acid 661 was elaborated and transformed into d62(Scheme LXV). Cyclization, thermal isomerization, and catalytic hydrogenation gave 657 and ultimately hirsutine. 

Saa and coworkers reported a remarkable cycloisomerization of alkynal to cycloalk-ene derivatives with loss of a CO molecule [30] some examples are shown in Table 6.3. Heating 5-alkynal 94a in AcOH (90 °C, 24h) with [Ru(Cp)(CH3CN)3]PF6 (5 mol%) afforded the cyclopentene derivative 9Sa in 90% yield. Ketone 94e afforded the cyclopentene 9Se in moderate yield, whereas the ester 94f gave the noncyclized product 96 with loss of one carbon unit (Table 6.3) (Scheme 6.32). 

Butene is oxidized to methyl ethyl ketone, presumably arizing from the acid-catalyzed rearrangement of the peroxide. Alkenols and aldehydes are formed in lower amounts. Cyclopentene is more reactive towards oxidation than butenes. 

Although the catalytic reactions described above involve mononuclear Rh and Rh complexes, dinuclear Rh compoimds have also been studied as catalyst precursors in oxygenation reactions. The system [Rh2(p.-OAc)4]/ f-BuOOH is effective in the oxidation of cyclic alkenes such as cyclopentene, cyclohexene and cycloheptene, mainly to o, /i-unsaturated ketones and allylic acetates, but with poor yields (Eq. 4) [30,31]. 

A plausible mechanism involves the reaction of the dihydride precursor with t-butylethylene to the 14-e complex [Ir(C6H3-2,6 CH2P-f-Bu2 2)]> which undergoes the oxidative-addition reaction of the alcohol to afford a hydride alkoxide complex. Further /i-hydride ehmination gives the alde-hyde/ketone and regenerates the dihydride active species [55]. In the particular case of 2,5-hexanediol as the substrate, the product is the cycHc ketone 3-methyl-2-cyclopenten-l-one. The formation of this ketone involves the oxidation of both OH groups to 2,5-hexanedione followed by an internal aldol reaction and further oxidation as in the final step of a Robinson annotation reaction [56]. 

Alkylidenes (alkylidene carbenes) are valence isomers of alkynes. They have been prepared by alkyne pyrolysis, by homologation of ketones, and by generation of alkenyl anions bearing oc-leaving groups. Generated by any of these means, an alkylidene will insert intramolecularly into a remote C- H bond to form a new C—C bond and thus a cyclopentene. A concerted two-electron process, this reaction proceeds with retention of absolute configuration at the C - H site. 

In 1982, it was reported that an aliphatic ketone, on exposure to dimethyl (diazometh-yl)phosphonate, is converted to the corresponding cyclopentene. c.g., the conversion of 2-methyl-5-nonanone to cyclopentencs 1 and 226. 

By a similar method, cyclopentanone reacts with dimethylamine to afford a 56 % yield (or an 87 % conversion based on ketone used) of dimethylamino-1-cyclopentene, b.p. 85°-86°C (104 mm), nj,5 1.4801. 

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