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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2262527Generated: November 4, 2026

Bromine → 2-Bromo-1-(3-phenyl-5-trifluoromethyl-isoxazol-4-yl)-ethanone

https://huagongshe.com/reaction/2262527

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
Reactant1-(3-Phenyl-5-trifluoromethyl-isoxazol-4-yl)-ethanoneHCID 67363403—
SolventAcetic AcidHCID 176—
SolventChloroformHCID 6212—
Product2-Bromo-1-(3-phenyl-5-trifluoromethyl-isoxazol-4-yl)-ethanoneHCID 8737039759.9%

Reaction Steps

To a solution of 1-(3-phenyl-5-trifluoromethyl-isoxazol-4-yl)-ethanone (2.88 g, 11 mmol) in chloroform (11 mL) and AcOH (0.6 mL) at 48° C. was added a solution of bromine (0.61 mL, 12 mmol) in chloroform (3.5 mL) over 5 min keeping the temperature below 50° C. After addition the reaction mixture was allowed to cool down to room temperature and poured into ice-water (200 mL). The layers were separated and the aqueous layer extracted with dichloromethane. The combined organic layers were then washed with water and brine, dried over sodium sulphate and evaporated. Purification by chromatography (SiO2, heptane:ethyl acetate: 100:0 to 4:1) afforded the title compound (2.2 g, 59%) which was obtained as a light yellow oil. MS: m/e=334.3/336.4 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07851469B2
Source datasetuspto-grants-2010_12
ORD IDord-3c40529d311e454db32dab8bf2b968e5
Source noteuspto-grants-2010_12