Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1086048Generated: November 1, 2026

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

https://huagongshe.com/reaction/1086048

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 numberUS05011992
Source datasetuspto-grants-1991_04
ORD IDord-fa7f4e50b60b49588499a4b6db992390
Source noteuspto-grants-1991_04