Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1758838Generated: November 1, 2026

2-Bromopropionic acid → HCID 53651654, compound

https://huagongshe.com/reaction/1758838

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromopropionic acidHCID 11729—
ReactantSodium HydroxideHCID 14798—
ReactantAlanine methyl ester hydrochlorideHCID 2733257—
Solvent1,4-Dioxane--water (1/1)HCID 21886435—
ProductHCID 53651654HCID 53651654—

Reaction Steps

Neutralize a solution of 1.4 g of methyl L-alaninate HCl and 3.1 g of α-bromopropionic acid in a dioxane-water mixture to pH 9 with sodium hydroxide. Warm to 70° and hold for 30 minutes, keeping the pH at 8 to 9 by addition of sodium hydroxide as necessary. Cool, apply to a column of Dowex 50 (H+) ion exchange resin, wash with water, and elute with 2% pyridine in water. Combine the product fractions and freeze dry. Purify this crude by chromatography on an ion-exchange column of Dowex 50 (Na+) in 0.5 M sodium citrate buffer pH 3.3. Collect the product fractions, concentrate to a small volume in vacuo, and repeat the Dowex 50 (H+) chromatography. Freeze dry the product fractions to obtain the pure N-(1-carbomethoxyethyl)-alanine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04374829
Source datasetuspto-grants-1983_02
ORD IDord-0a713b2a6f674c8b9aa17b4e01cba33a
Source noteuspto-grants-1983_02