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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2163814Generated: November 2, 2026

Water → N-methyl-N-propionyl-L-alanine methyl ester

https://huagongshe.com/reaction/2163814

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantPropionic anhydrideHCID 31263—
ReactantN-Methyl-L-alanine methyl ester hydrochloride (1:1)HCID 13850987—
SolventChloroformHCID 6212—
SolventEthyl AcetateHCID 8857—
ProductN-methyl-N-propionyl-L-alanine methyl esterHCID 53825128—

Reaction Steps

In 150 ml of chloroform was dissolved 28 g (0.18 mol) of N-methyl-L-alanine methyl ester hydrochloride, followed by addition of 27 g (0.21 mol) of propionic anhydride and 33 ml of triethylamine. The mixture was allowed to stand at room temperature overnight. With the addition of 100 ml of water, the reaction mixture was stirred at room temperature for 30 minutes. Thereafter, 600 ml of ethyl acetate was added and the organic layer was washed with aqueous sodium hydrogen carbonate and water in the order mentioned, and dried over anhydrous sodium sulfate. The solvent was removed under reduced pressure. In the above manner, N-methyl-N-propionyl-L-alanine methyl ester was obtained as a yellow oil. NMR spectrum (CDCl3) δ: 1.15(3H,t,J=7Hz), 1.40(3H,d,J=7Hz), 2.40(2H,q,J=7Hz), 2.93(3H,s), 3.70(3H,s), 5.27(1H,q, J=7Hz)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04137230
Source datasetuspto-grants-1979_01
ORD IDord-5c29aabdfa0c4027b6f87eb90a45d80e
Source noteuspto-grants-1979_01