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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 620278Generated: October 30, 2026

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

https://huagongshe.com/reaction/620278

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 numberUS04820715
Source datasetuspto-grants-1989_04
ORD IDord-eec40a5104f54b0dbe9ac58825ade751
Source noteuspto-grants-1989_04