HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzeneacetic acid, .alpha.-ethyl-, ethyl ester → HCID 23453027, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzeneacetic acid, .alpha.-ethyl-, ethyl ester | HCID 97713 | — |
| Reactant | HCID 23453105 | HCID 23453105 | — |
| Product | HCID 23453027 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04207341 |
| Source dataset | uspto-grants-1980_06 |
| ORD ID | ord-2d6423c3278a4f5e9893a9e1f8cc26c6 |
| Source note | uspto-grants-1980_06 |