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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1912426Generated: October 31, 2026

Thionyl Chloride → [Benzyl-(2-chloro-1-methylethyl)-amino]acetic acid tert-butyl ester

https://huagongshe.com/reaction/1912426

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantSodium BicarbonateHCID 516892—
Reactant[Benzyl-(2-hydroxy-1-methylethyl)-amino]acetic acid tert-butyl esterHCID 58293285—
SolventChloroformHCID 6212—
Product[Benzyl-(2-chloro-1-methylethyl)-amino]acetic acid tert-butyl esterHCID 58293349—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of an optically-active compound of [benzyl-(2-hydroxy-1-methylethyl)-amino]acetic acid tert-butyl ester (160.0 g) in chloroform (640 ml) cooled to 0° C. was added dropwise thionyl chloride (50.0 ml), and the mixture was stirred at 60° C. for 2 hours. The reaction mixture was cooled to 0° C. Then, thereto were added saturated aqueous sodium bicarbonate solution (1000 ml) and chloroform (100 ml), and the mixture was stirred. The separated organic layer was washed with saturated aqueous sodium chloride solution (500 ml), and the aqueous layer was extracted with chloroform (450 ml) again. The combined organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure to give the titled compound (172.9 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609647B2
Source datasetuspto-grants-2013_12
ORD IDord-4197bcef3b754de489e2486bb8ec9e1a
Source noteuspto-grants-2013_12