Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1382979Generated: October 31, 2026

1-Acetoxy-2-bromoethane → HCID 14372575, compound

https://huagongshe.com/reaction/1382979

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Acetoxy-2-bromoethaneHCID 13564—
Reactanto-Desmethyl metoclopramideHCID 9817332—
SolventAcetonitrileHCID 6342—
ProductHCID 14372575HCID 1437257585.5%

Reaction Steps

A solution of the tetrabutylammonium salt of 4-amino-5-chloro-N-[2-(diethylamino)ethyl]-2-hydroxybenzamide (5.27 g, 10 mmoles) (prepared in Preparation No. 3) in acetonitrile (100 ml) and 2-bromoethylacetate (2 g, 12 mmoles) was stirred for 48 hours. The solvent was evaporated and the residue partitioned between ethyl acetate and water. The organic layer was washed with ice-cold 0.4N sodium hydroxide solution, water, dried and the solvent evaporated. The residue was chromatographed over deactivated silica using methylene chloride (100), methanol (2), ammonia (0.5) solvent system. The appropriate fractions were combined and the solvent evaporated to leave a residue of 3.18 g (85%) of the title compound. Crystallization from toluene gave a sample, mp. 101°-102° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04808624
Source datasetuspto-grants-1989_02
ORD IDord-a7903e47ea5b4ace96f0dccbe1acce7d
Source noteuspto-grants-1989_02