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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 731668Generated: October 30, 2026

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

https://huagongshe.com/reaction/731668

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
Reactant1-(5-Cyclopropyl-3-phenyl-isoxazol-4-yl)-ethanoneHCID 67421136—
SolventAcetic AcidHCID 176—
SolventCarbon TetrachlorideHCID 5943—
Product2-Bromo-1-(5-cyclopropyl-3-phenyl-isoxazol-4-yl)-ethanoneHCID 2473980796%

Reaction Steps

To a solution of 1-(5-cyclopropyl-3-phenyl-isoxazol-4-yl)-ethanone (3.34 g, 14.6 mmol) in carbontetrachloride (9.7 mL) and AcOH (0.4 mL) at 48° C. was added a solution of bromine (0.79 mL, 14.6 mmol) in carbontetrachloride (7.8 mL) over 10 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 (50 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 80:20) afforded the title compound (4.29 g, 95%) which was obtained as an off-white solid. MS m/e (EI): 305.0/307.0 [M].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07585874B2
Source datasetuspto-grants-2009_09
ORD IDord-b2e60627a8294d0a8461175471cc4634
Source noteuspto-grants-2009_09