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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1912427Generated: October 31, 2026

Water → [Benzyl-(2-chloropropyl)-amino]acetic acid tert-butyl ester

https://huagongshe.com/reaction/1912427

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDimethylformamideHCID 6228—
Reactant[Benzyl-(2-chloro-1-methylethyl)-amino]acetic acid tert-butyl esterHCID 58293349—
Product[Benzyl-(2-chloropropyl)-amino]acetic acid tert-butyl esterHCID 58293274—

Reaction Conditions

Temperature80 °C

Reaction Steps

An optically-active compound of [benzyl-(2-chloro-1-methylethyl)-amino]acetic acid tert-butyl ester (172.9 g) was dissolved in N,N-dimethylformamide (520 ml), and stirred at 80° C. for 140 minutes. The reaction mixture was cooled to 0° C. Then, thereto was added water (1200 ml), and the mixture was extracted with n-hexane/ethyl acetate (2/1, 1000 ml). The organic layer was sequentially washed with water (700 ml) and saturated aqueous sodium chloride solution (400 ml), and the separated aqueous layer was extracted with n-hexane/ethyl acetate (2/1, 600 ml) again. The combined organic layer was concentrated under reduced pressure, and the resulting residue was purified by silica gel column chromatography (eluent: n-hexane/ethyl acetate=50/1 to 40/1) to give the titled compound (127.0 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609647B2
Source datasetuspto-grants-2013_12
ORD IDord-52cafdcaf7844865ac55bdbdd3f9af04
Source noteuspto-grants-2013_12