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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1723265Generated: November 1, 2026

Methyl chloroacetate → N-(3,5-difluorobenzyl)-glycine methyl ester

https://huagongshe.com/reaction/1723265

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl chloroacetateHCID 7295—
ReactantTriethylamineHCID 8471—
Reactant3,5-DifluorobenzylamineHCID 145211—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
ProductN-(3,5-difluorobenzyl)-glycine methyl esterHCID 1447994341%

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of 3,5-difluorobenzylamine prepared as above (12.3 g, 0.0863 mole), methyl chloroacetate (7.6 ml, 0.0863 mole) and triethylamine (12.0 ml, 0.0863 mole) in dry dimethylformamide (85 ml) was heated at 60° C. for 3 hours. The mixture was diluted with an equal volume of ether and the triethylamine hydrochloride filtered. The filtrate was concentrated under vacuum, the resultant oil triturated with ethyl acetate, and the solution decanted from a small amount of residual oil. The solvent was removed and the product was purified by flash chromatography (silica) by eluting with hexane-ethyl acetate (70:30) to give N-(3,5-difluorobenzyl)glycine methyl ester as an oil (7.61 g, 41%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04859779
Source datasetuspto-grants-1989_08
ORD IDord-26b77a5fc37e42eeac584b313a17423a
Source noteuspto-grants-1989_08