Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1626003Generated: November 2, 2026

Chloroacetyl chloride → HCID 67078123, compound

https://huagongshe.com/reaction/1626003

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
ReactantTriethylamineHCID 8471—
Reactant2-Amino-3-(benzyloxy)propan-1-olHCID 14118408—
SolventMethanolHCID 887—
SolventAcetonitrileHCID 6342—
ProductHCID 67078123HCID 67078123—

Reaction Conditions

Temperature-10 °C

Reaction Steps

(2R)-2-Amino-3-(benzyloxy)propan-1-ol (2.18 g) was dissolved in acetonitrile (38 ml) and methanol (7 ml), and triethylamine (2.0 ml) was added. The atmosphere was replaced with nitrogen, and then the mixture was cooled to −10° C. A solution of chloroacetyl chloride (1.05 ml) in acetonitrile (9 ml) was added dropwise thereto, and the mixture was stirred for 20 hours to be gradually warmed to room temperature. The reaction solvent was distilled off, and the residue was directly purified by silica gel column chromatography (developed with ethyl acetate-hexane) to give the title compound (2.26 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785438B2
Source datasetuspto-grants-2014_07
ORD IDord-82063818d3194f4b8a6247a5dd49b930
Source noteuspto-grants-2014_07