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Crotonic acid, /3-hydroxy

CROTONIC ACID, 3-HYDROXY-, MEHYL ESTER, DIMETHYL PHOSPHATE DIMEHYL(1-METHOXYCARBOXYPROPEN-2-YL)PHOSPHATE DIMETHYL 2-METHOXYCARBONYL-1-METHYLVINYL PHOSPHATE DIMETHYL METHOXYCARBONYLPROPENYL PHOSPHATE DIMETHYL-1 -CARBOMETHOXY-1-PROPEN-2-YL PHOSPHATE DURAPHOS... [Pg.16]

Isocroionic acid, -crotonic acid, cis-croionic acid. Colourless needles m.p. 14 C, b.p. 169 C. Prepared by distilling -hydroxy-glutaric acid under reduced pressure. Converted to a-crotonic acid by heating at 180 C, or by the action of bromine and sunlight on an aqueous solution. [Pg.116]

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. [Pg.335]

The fraction, x, of -hydroxy crotonic acid that isomerizes into acetoacetic ester was measured at 25°C at various times. The data indicate reversibility. Find the rate equation. [Pg.137]

DL-Threonic acid (10) seemed to be a promising source of DL-threose. Therefore, other routes to 10 were elaborated. By a procedure consisting of five steps" 2-propenal (acrolein) — vinylglycoloni-trile — ethyl vinylglycolate — ethyl 4-bromocrotonate — 3-hydroxy-crotonic acid — 10, DL-threonic acid was obtained in an overall yield of 4.1%. Another synthesis of 10 was achieved17 in six steps starting... [Pg.5]

Adams and Reifschneider 22 have reported ring opening and formation of 6-hydroxypyridine-2-crotonic acid by strong alkaline or acid hydrolysis of 6-hydroxy-4-quinolizone with ester groups in the 1-and 3-positions. However, hydrolysis with barium oxide affords the corresponding l-carbethoxy-3-carboxy-6-hydroxy-4-quinolizone. [Pg.306]

Benzene may be alkylated by certain unsaturated, halo, hydroxy, and keto acids. The yields of phenyl-substituted acids are usually low (18-65%). In the alkylation of benzene by cinnamic and crotonic acids the major products are 3 phenyl- and 3-methyl-hydrindones, respectively, formed by subsequent ring closures by Friedel-Crafts acylation. ... [Pg.222]

Reaction of a,P-unsaturated acids with ketones Lithium naphthalenide in the presence ofdiethylamine reacts with x,/ -unsaturated adds, for examplecrotonic acid (1), to give the a-anion of lithium crotonate. This anion reacts with ketones, for example cyclohexanone (2), to give d-hydroxy acids, for example 5(r-hydroxycyclohex-r-yl)-crotonic acid (3). [Pg.348]

DIMETHOXYPHOSPHINYL)OXY)-, METHYL ESTER 2-BUTENOIC ACID 3-((DIMETHOXYPHOSPHINYL)OXY)-2-BUTENOIC ACID METHYL ESTER 3-HYDROXY-. METHYL ESTER. DIMETHYL PHOSPHATE CROTONIC ACID 3-HYDROXYCROTONIC ACID METHYL ESTER DIMETHYL PHOSPHATE 3-( DIMETHOXYPHOSPHINYL)-, METHYL ESTER 2-BUTENOIC ACID... [Pg.16]

Mupirocin calcium cream 2% contains the dihydrate crystalline calcium hemisalt of the antibiotic mupirocin. Chemically, it is ((alpha) E,2 5,3 R,4 R,5 5)-5-[(2 5,3 5,4 5,5 5) -2,3 -epoxy-5-hydroxy-4-methylhexyl]tetra-hydro-3, 4-dihydroxy-(beta)-methyl-2//-pyran-2-crotonic acid, ester with 9-hydroxynonanoic acid, calcium salt (2 1),... [Pg.209]

A stream of air, charged with bromine vapor, introduced into a vigorously stirred 0.34 M aq. soln. of crotonic acid over a period of 5 hrs., then air bubbled rapidly through the reaction mixture for an additional 30 min. to remove any excess bromine —a-bromo- -hydroxy-n-butyric acid. Y 79%. (H. E. Carter and C. L. Zirkle, J. Biol. Chem. 178, 709 (1949).). ... [Pg.147]

An ethereal soln. of diethylamine added to an ethereal soln. of methyl 3-hydroxy-3-phenyl-l-propyne-l-carboxylate at 0°, and allowed to stand overnight at the same temp. —> -diethylamino-y-hydroxy-y-phenyl crotonic acid lactone. Y 70% (cf. Synth. Meth. 5, 57). (A. W. Nineham and R. A. Raphael, Soc. 1949, 118 also / -alkoxy derivatives s. E. R. H. Jones and M. C. Whiting, Soc. 1949, 1423.)... [Pg.355]

E)-(2S,3R,4R,5S)-5-([(2S,3S,4S,5S)-2,3-Epoxy-5-hydroxy-4-methylhexyl]tetrahydro-3,4-dihydroxy-p-methyl-2H-pyran-2-crotonic acid ester with 9-hydroxynonanoic acid. [Pg.425]

The hydroxy-acid (53), an intermediate in vitamin A synthesis, has been prepared in 51 % yield from )9-ionone and crotonic acid using lithium naphthal-enide. ... [Pg.240]

Ethyl 4-hydroxycrotonate Crotonic acid, 4-hydroxy-, ethyl ester, (E)- (8) ... [Pg.170]

Other Names 2(5H)-Furanone, S.S-fcwCp-hydroxyphenyl)- Crotonic acid, 4- hydroxy-4, (p-hydroxyphenyl)-, y-lactone Phenolmalein CA Index Name 2(5H)-Fnranone, 5,5- j5 (4-hydroxyphenyl)-CAS Registry Number 1224-25-5 Merck Index Number Not listed Chemical Structure... [Pg.301]

The orthovanadate-catalysed epoxidation of crotonic acid with H2O2 is zero order in H202. The oxidations and disproportionations of 3-hydroxy-2,4,6-trinitrophenol (TNR), 2-mono-nitrophenol (MNP), 2,4-dinitrophenol (DNP), and 2,4,6-trinitrophenol (TNP) promoted by Fenton reagent at pH = 3.1 have been studied. The reaction characteristics were studied by measuring concentration changes of dissolved organic carbon over time instead of measuring nitrophenol content for each specific compound. ... [Pg.145]

Diethylamine added at -30° to a soln. of Li-naphthalene prepared from Li and naphthalene in tetrahydrofuran, then crotonic acid in tetrahydrofuran added drop-wise at - 5° followed by cyclohexanone, and heated 1.5 hrs. at 60° y-(l-hydroxy-... [Pg.162]


See other pages where Crotonic acid, /3-hydroxy is mentioned: [Pg.149]    [Pg.149]    [Pg.112]    [Pg.62]    [Pg.338]    [Pg.116]    [Pg.57]    [Pg.105]    [Pg.126]    [Pg.203]    [Pg.67]    [Pg.107]    [Pg.160]    [Pg.54]    [Pg.576]    [Pg.54]    [Pg.105]    [Pg.132]    [Pg.135]    [Pg.161]    [Pg.388]    [Pg.36]    [Pg.96]    [Pg.44]    [Pg.305]    [Pg.307]    [Pg.124]   
See also in sourсe #XX -- [ Pg.126 ]

See also in sourсe #XX -- [ Pg.126 ]




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Crotonate

Crotonates

Crotonic

Crotonic acid

Crotonization

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