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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2226387Generated: October 31, 2026

Ethyl alpha-oxobenzenebutanoate → Ammonium Hydroxide

https://huagongshe.com/reaction/2226387

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl alpha-oxobenzenebutanoateHCID 562087—
ReactantHCID 13146116HCID 13146116—
SolventMethanolHCID 887—
ProductAmmonium HydroxideHCID 149237%
ProductHCID 67788181HCID 67788181—

Reaction Steps

Dissolve 1-[(S)-alanyl ]octahydroindole-2(S)-carboxylic acid (prepared in paragraph D of this example) in 100 ml of absolute methanol. Add 1.10 g 2-oxo-4-phenylbutyric acid, ethyl ester and 20 ml of 3 Angstrom molecular sieve pellets, and stir the resulting mixture at room temperature for eighteen hours. Filter the reaction mixture and treat the filtrate with 0.68 g sodium cyanoborohydride at room temperature for two hours. Concentrate the mixture under nitrogen and dilute the oil with dilute hydrochloric acid and stir at room temperature for one hour. Absorb the aqueous solution on 200 ml of a XAD-2 (Rohm & Haas-Co. resin). Elute the resin with 2000 ml of water and then with 2000 ml of methanol. Concentrate the methanol solution and place the residue on a column of silica gel (400 g, 60-200 mesh) and elute with chloroform:isopropanol: 7% ammonium hydroxide 1:1:1 (organic layer) to give 1-[N-(1-methoxycarbonyl-3-phenyl propyl)-(S)-alanyl]octahydroindole-2(S)-carboxylic acid, a white solid [ α]D26 -45.3° (ethanol), m.p. 71°-73°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05348944
Source datasetuspto-grants-1994_09
ORD IDord-c2b1a86ea7614279aba6c39bba0f034c
Source noteuspto-grants-1994_09