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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2226422Generated: October 30, 2026

Methyl 2-oxo-4-phenylbutanoate → Ammonium Hydroxide

https://huagongshe.com/reaction/2226422

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 2-oxo-4-phenylbutanoateHCID 11805548—
Reactant1-[(S)-alanyl]hexahydrofuro[3,4-b]pyrrole-2(S)-carboxylic acidHCID 18654890—
SolventMethanolHCID 887—
ProductAmmonium HydroxideHCID 149237%
Product1-[N-(1-carbomethoxy-3-phenylpropyl)-(S)-alanyl]hexahydrofuro[3,4-b]pyrrole-2(S)-carboxylic acidHCID 67852435—

Reaction Steps

Dissolve 1-[(S)-alanyl]hexahydrofuro[3,4-b]pyrrole-2(S)-carboxylic acid (prepared in paragraph C of this example) in absolute methanol. Add 2-oxo-4-phenylbutyric acid, methyl ester and 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 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 XAD-2 (Rohm & Hass Co.) resin. Elute the resin with water and then with methanol. Concentrate the methanol solution and place the residue on a column of silica gel and elute with chloroform:isopropanol: 7% ammonium hydroxide 1:1:1 (organic layer) to give 1-[N-(1-methoxycarbonyl-3-phenylpropyl)-(S)-alanyl]hexahydrofuro[3,4-b]pyrrole-2(S)carboxylic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05348944
Source datasetuspto-grants-1994_09
ORD IDord-06e12bcbb9ce4dbf993556ae715611da
Source noteuspto-grants-1994_09