Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Succinic anhydride synthesis

Synthesis of 3,4-benzpyrene (7). Improvements in the succinic anhydride synthesis of this potent carcinogen have already raised the yield from the original 3 % of Cook... [Pg.414]

Anthracene. IsraeU chemists have modified the Haworth succinic anhydride synthesis of phenanthrenes to a synthesis of anthracene. Thus treatment of the ketone (1) with PPA at 140° for an extended period results in formation... [Pg.474]

Haller-Bauer reaction, 525 a-Halo acyl chlorides, 75 2-Haloethyl esters, 553 y-Halo ketones, 524 Halomcthyl aryl ketones, 103 Halomethyl aryl sulfones, 41 Halomethylation, 105 tj-Halo-l-phenyl-l-alkynes, 165 Halopropyl isocyanates, 570 2-Halopyridines, 479 Halo-a,p-unsaturated ketones, 647-648 p-Halovinyl ketones, 644 Haworth succinic anhydride synthesis, 474 Hemithioacetal interchange, 381-382... [Pg.375]

A further example is given below illustrating the use of a dibasic anhydride (succinic anhydride) the succinoylation reaction is a valuable one since it leads to aroyl carboxylic acids and ultimately to polynuclear hydrocarbons. This general scheme of synthesis of substituted hydrocarbons through the use of succinic anhydride is sometimes called the Haworth reaction. Thus a-tetralone (see below) may be reduced by the Clemmensen method to tetralin (tetrahydronaphthalene) and the latter converted into naphthalene either catal3d.ically or by means of sulphur or selenium (compare Section, VI,33). [Pg.726]

Succineins. Succineins are carboxyethyl-substituted pyronines made by substituting succinic anhydride for formaldehyde in the basic synthesis,... [Pg.399]

With the saturated analogs, i.e. succinic anhydride and its derivatives, pyridazines are formed in only a few cases. The reaction has been applied to the preparation of perhydro-pyridazines and their 3,6-diones (68MI21200, 70JOC1468). For the synthesis of 4,5-dihalopyridazinones, /3-formylacrylic acids, for example mucochloric acid, are useful syn-thons (Scheme 80). [Pg.46]

The preferred catalysts are salts of inorganic and organic acids as well as tertiary amines. Phthalic anhydride, succinic anhydride and maleic anhydride are typical acid anhydrides, while ethylene oxide, propylene oxide, epichlorohydrin and phenyl glycidyl ether are typical epoxides. The synthesis of a ladder polymer was carried out by using bisanhydrides264. ... [Pg.22]

Hydroxamic acids are an important class of compounds targeted as potential therapeutic agents. A-Fmoc-aminooxy-2-chlorotrityl polystyrene resin 61 allowed the synthesis and subsequent cleavage under mild conditions of both peptidyl and small molecule hydroxamic acids (Fig. 14) [70]. An alternative hydroxylamine linkage 62 was prepared from trityl chloride resin and tV-hydroxyphthalimide followed by treatment with hydrazine at room temperature (Scheme 30) [71]. A series of hydroxamic acids were prepared by the addition of substituted succinic anhydrides to the resin followed by coupling with a variety of amines, and cleavage with HCOOH-THF(l 3). [Pg.203]

Af-(ter -Butoxycarbonyl)-3-hydroxymethylpiperidine is a building block in the synthesis of a potent tryptase inhibitor. It is produced by stereospecific esterification of the racemic alcohol with succinic anhydride [30]. The enzymatic resolution is followed up by separation of... [Pg.84]

Figure 7.20 The synthesis of alkenyl succinic anhydride (ASA) via the ene reaction between maleic anhydride and catalytically isomerised alk-l-enes. Figure 7.20 The synthesis of alkenyl succinic anhydride (ASA) via the ene reaction between maleic anhydride and catalytically isomerised alk-l-enes.
A low yield of y-oxo-4-dibenzothiophenebut3rric acid has been obtained by treatment of 4-lithiodibenzothiophene with succinic anhydride. Optimization of this reaction would enable the synthesis of y-oxo-1- and y-oxo-3-dibenzothiophenebutyric acid to be undertaken from the appropriate bromodibenzothiophenes. [Pg.278]

The diacylation of isopropenyl acetate with anhydrides of dicarboxylic acids is applicable for the synthesis of several other cyclic jS-triketones in moderate yield. - It has been used for the synthesis of 2-acetylcyclohexane-l,3-dione (40% yield), 2-acetyl-4-methylcyclopentane-l,3-dione (10% yield), 2-acetyl-4,4-dimethylcyclopentane-l,3-dione (10% yield), 2-acetyl-5,5-dimethylcyclohexane-l,3-dione (10% yield), 2-acetylcyclo-heptane-l,3-dione (12% yield) and 2-acetylindane-l,3-dione (26% yield). Maleic anhydrides under more drastic conditions give acetylcyclopent-4-ene-l,3-diones in yields from 5% to 12%. The corresponding acylation of the enol acetate of 2-butanone with succinic anhydride has been used to prepare 2-methylcyclopentane-l,3-dione, an important intermediate in steroid synthesis. - ... [Pg.3]

The synthesis of a water-soluble diphenylmethano-bridged fullerene 122 was achieved by hydrolyzing the bis (acetamide) 121 with acetic acid-aqueous hydrochloric acid and then converting it into the bis(succinamide) 122 by treatment with succinic anhydride (Scheme 4.25) [158]. Compound 122 is soluble in water at pH > 7. This is an important requirement for the investigation of the biological activity of fullerenes. Remarkably, 122 is an inhibitor for the HIV enzymes protease (HIV-P) and reverse transcriptase (HIV-RT) [159]. As suggested by molecular modeling. [Pg.125]

The first agent of this class to be introduced in the clinic, haloperidol (18-8), interestingly shares the 4-phenylpiperidine structural fragment found in the central analgesic agent meperidine and its derivatives (see Chapter 7). The former compound may well have been discovered in the course of further SAR studies on the opiate [20]. An unusual synthesis of haloperidol starts with the product (18-1) from Friedel-Crafts acylation of 4-fluorobenzene with succinic anhydride. Successive protection of the... [Pg.332]

S)-N-(tert-butoxycarbonyl)-hydroxymethylpiperidine (8) is a key intermediate in the synthesis of a potent tryptase inhibitor (Scheme 7.5). It was synthesized from (R,.S)-3-hydroxyrnethylpiperidine via fractional crystallization of the corresponding L(-)dibenzoyl tartrate salt followed by hydrolysis and acylation [17]. The lipase from Pseudomonas cepacia (PS-30) immobilized on polypropylene accurel PP catalyzed the esterification of racemic 6 with succinic anhydride and toluene, giving the (S)-hemisuccinate ester (7). This was easily separated and hydrolyzed by base to the (S)-Boc-protected 3-hydroxymethylpiperidine (8). Using this repeated esterification procedure gave a 32% yield (maximum theoretical yield = 50%) and 98.9% . [Pg.172]

Methyl- 1,3-cyclopentanedione is a key intermediate for the total synthesis of steroids.2 A number of methods have been described for its preparation, among them the condensation of succinic acid with propionyl chloride,3 and that of succinic anhydride with 2-buten-2-ol acetate,4 both in the presence of aluminum chloride. It has also been obtained from 3-methylcyclopentane-1,2,4-trione by catalytic hydrogenation5 and Wolff-Kishner reduction 6 The base-promoted cyclization of 4-oxohexanoic acid ethyl ester and diethyl propionylsuccinate with tertiary alkoxides was first reported by Bucourt.7 The present cyclization process provides an experimentally simple route to 2-methyl-1,3-cyclopentanedione. Using the same procedure, 4-oxoheptanoic acid ethyl ester has been cyclized to give 2-ethyl-l,3-cyclopentanedione in 46% yield... [Pg.85]

Sodium toluene dispersion of, 55, 65 Sodium p-toluenesulfinate, 57, 103 Spiro[4 n] alkenones, 58, 62 Spiro[cyclopentane-l,l -indene] 55, 94 Squalene, 56, 116 Squalene, 2,3-epoxy, 56, 116 Stannic chloride, 56, 97 Steroids synthesis, 58, 85 E Stilbene, 55, 115,58, 73 z-Stilbene, 58, 133 Styrene, 56, 35,58, 43 Styrene glycol, 55, 116 Styrene glycol dimesylate, 55, 116 Succinic acid, 58, 85 Succinic anhydride, 58, 85 Sucunimide, 56, 50, 58, 126 Succimmide, Vbromo, 55, 28, 56, 49 SULFIDE CONTRACTION, 55, 127 Sulfide, dimethyl-, 56, 37 SULFIDE SYNTHESIS, 58, 143,58, 138 SULFIDE SYNTHESIS ALKYL ARYL SULFIDES, 58, 143 SULFIDE SYNTHFSIS DIALKYL SULFIDES, 58, 143 SULFIDE SYNTHESIS UNSYMMETRI-CAL DIALKYL DISULFIDES, 58, 147 SULFONYL CYANIDES, 57, 88 Sulfur tetrafluoride, 57, 51... [Pg.192]

Synthesis Fenbufen is prepared by the Friedel-Crafts (aluminum chloride-nitrobenzene) acylation of biphenyl with succinic anhydride (Tomcufcik et al. (American Cyanamid Co.), 1972). [Pg.59]


See other pages where Succinic anhydride synthesis is mentioned: [Pg.680]    [Pg.680]    [Pg.110]    [Pg.140]    [Pg.102]    [Pg.276]    [Pg.153]    [Pg.300]    [Pg.32]    [Pg.50]    [Pg.484]    [Pg.496]    [Pg.301]    [Pg.396]    [Pg.685]    [Pg.362]    [Pg.606]    [Pg.206]    [Pg.22]    [Pg.885]    [Pg.905]   
See also in sourсe #XX -- [ Pg.2 , Pg.607 ]

See also in sourсe #XX -- [ Pg.2 , Pg.607 ]




SEARCH



2- succinic anhydrid

Anhydride synthesis

Haworth succinic anhydride synthesis

Succinates, synthesis

Succinic anhydride

Synthesis succinate

© 2024 chempedia.info