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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1706489Generated: October 29, 2026

Benzeneacetic acid, .alpha.-ethyl-, ethyl ester → HCID 23453027, compound

https://huagongshe.com/reaction/1706489

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneacetic acid, .alpha.-ethyl-, ethyl esterHCID 97713—
ReactantHCID 23453105HCID 23453105—
ProductHCID 23453027HCID 23453027—

Reaction Steps

For the preparation of ethyl 2-[4-(2-aminoethyl)-phenyl]-butyrate hydrochloride, ethyl 2-phenylbutyrate is chloromethylated and the ethyl 2-(p-chloromethylphenyl)-butyrate obtained (b.p. 117°-123° C./0.2 mm Hg) is reacted with potassium cyanide in acetone to give ethyl 2-(p-cyanomethylphenyl)-butyrate (b.p. 156°-160° C./0.3 mm Hg). By the catalytic hydrogenation of the nitrile group in the presence of a palladium/charcoal catalyst in alcoholic hydrochloric acid solution, there is obtained ethyl 2-[4-(2-aminoethyl)-phenyl]-butyrate hydrochloride, which does not crystallize.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04207341
Source datasetuspto-grants-1980_06
ORD IDord-2d6423c3278a4f5e9893a9e1f8cc26c6
Source noteuspto-grants-1980_06