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Ethyl 3-phenylpropionate

Ethyl phenylacetate, reaction with (2-bromoethyl)benzene, 47, 72 Ethyl 2-phenylhexanoate, 47, 74 Ethyl 2-phenylpropionate, 47, 74 Exchange of oxygen by sulfur in preparation of chloromethylphospho-nothioic dichlonde, 46, 21 Extractor, stirred in isolation of 3-hydroxyglutaromtnle, 46, 49... [Pg.129]

Scrophularia aurtcujaia Scropolioside A Scrovalcntinoside Anti-inflammatory against ethyl-phenylpropionate-induced edema Active. Active. [1201... [Pg.379]

The condensation of naphthalenc-1,8-diamine (17) with several /8-oxo esters gives 1,5-diazocine derivatives. An example is the reaction of 17 with ethyl 3-oxo-3-phenylpropionate.39... [Pg.544]

C5H9NO 10431-98-8) see Nefazodone hydrochloride ( )-ethyl 2-oxo-3-benzoylamino-3-phenylpropionate (C H,7N04 153433-79-5) see Paclitaxel ethyl 3-oxocaproatc... [Pg.2383]

CHLOROCYCLOBUTANE, 51, 106 Mesitylene, cyanation, 50, 54 METHALATION OF 2-METHYLPYRIDINE DERIVATIVES ETHYL 6-METHYL-PYRIDINE-2-ACETATE, 52, 75 Metalation, directed, 53, 59 Methallyl alcohol, with phenyl-mercuric acetate to yield 2-methyl-3-phenylpropional-dehyde, 51, 17 METHALLYLBENZENE, 52, 115 7r-Methallylnickel bromide, 52, 115... [Pg.61]

In ethyl 3-keto-2-oximino-3-phenylpropanoate catalytic hydrogenation over palladium on carbon reduced both the keto and oximino group, giving a 74% yield of ethyl ester of -phenylserine (ethyl 2-amino-3-hydroxy-3-phenylpropionate). The reduction is stereospecific and only the erythro dia-stereomer was obtained, probably via a cyclic intermediate 11097]. Similarly, hydrogenation over Raney nickel at 25-30° and 1-3 atm converted ethyl a-oximimoacetoacetate quantitatively to ethyl 2-amino-3-hydroxybutanoate [45]. [Pg.163]

Ethyl <2,/3-dibromo-/3-phenylpropionate is prepared by adding bromine to ethyl cinnamate.1... [Pg.37]

A solution of potassium hydroxide is prepared by dissolving 252.5 g. (4.5 moles) of potassium hydroxide (Note r) in 1200 cc. of 95 per cent alcohol contained in a 3-I. round-bottom flask provided with a reflux condenser and heated on a steam bath. To the alkaline solution, cooled to 40-50°, is added 336 g. (x mole) of crude ethyl <, /3-dibromo-/3-phenylpropionate (p. 37). When the initial reaction has subsided, the contents of the flask are refluxed for five hours on the steam bath. [Pg.60]

See other pages where Ethyl 3-phenylpropionate is mentioned: [Pg.605]    [Pg.290]    [Pg.398]    [Pg.432]    [Pg.442]    [Pg.444]    [Pg.398]    [Pg.421]    [Pg.423]    [Pg.425]    [Pg.425]    [Pg.432]    [Pg.441]    [Pg.442]    [Pg.443]    [Pg.444]    [Pg.389]    [Pg.236]    [Pg.247]    [Pg.608]    [Pg.776]    [Pg.374]    [Pg.111]    [Pg.41]    [Pg.236]    [Pg.89]    [Pg.90]    [Pg.693]    [Pg.2376]    [Pg.2376]    [Pg.2383]    [Pg.2434]    [Pg.2447]    [Pg.2447]    [Pg.776]    [Pg.589]    [Pg.146]    [Pg.6]    [Pg.213]    [Pg.213]   
See also in sourсe #XX -- [ Pg.47 , Pg.74 ]

See also in sourсe #XX -- [ Pg.47 , Pg.74 ]



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