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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1616641Generated: October 31, 2026

2-Bromo-1-[2-(trifluoromethyl)phenyl]ethan-1-one → 5-[4-(2-Trifluoromethyl-phenyl)-oxazol-2-yl]-pentanoic acid methyl ester

https://huagongshe.com/reaction/1616641

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-1-[2-(trifluoromethyl)phenyl]ethan-1-oneHCID 2778430—
ReactantMethyl 6-amino-6-oxohexanoateHCID 14266897—
SolventWaterHCID 962—
Product5-[4-(2-Trifluoromethyl-phenyl)-oxazol-2-yl]-pentanoic acid methyl esterHCID 59167779—

Reaction Steps

Combine 2-bromo-1-(2-trifluoromethyl-phenyl)-ethanone (6.6 g, 24.7 mmol) with 5-carbamoyl-pentanoic acid methyl ester (7.8 g, 49 mmol) and heat the neat mixture in a sealed vessel at 140-150° C. for about 4.5 hours. Cool the mixture, dilute with water, and extract with EtOAc. Dry the combined extracts over Na2SO4 and concentrate. Chromatography over silica gel (CH2Cl2) allows for recovery of 5-[4-(2-trifluoromethyl-phenyl)-oxazol-2-yl]-pentanoic acid methyl ester (3.47 g, 43%). MS (ES): (M+1)+ 328.2 m/z.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765796B2
Source datasetuspto-grants-2014_07
ORD IDord-754cf584ad4c4c8e9385fff9a6b02e0b
Source noteuspto-grants-2014_07