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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 895331Generated: October 28, 2026

Bromine → 1-[4-(Benzyloxy)phenyl]-2-bromoethan-1-one

https://huagongshe.com/reaction/895331

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
Reactant1-[4-(Benzyloxy)phenyl]ethan-1-oneHCID 245226—
SolventChloroformHCID 6212—
Product1-[4-(Benzyloxy)phenyl]-2-bromoethan-1-oneHCID 10542593—

Reaction Steps

Bromination of 4′-benzyloxyacetophenone (step 2) Bromine (80 mmol) was added dropwise over 5 min to a stirred solution of 4′-benzyloxyacetophenone (70 mmol) in 40 ml chloroform. This mixture was stirred for an additional 5 min and quenched with saturated sodium bicarbonate in water until the pH reached 7. The organic layers were combined, dried over MgSO4, and concentrated to dryness. The crude mixture was purified over a silica gel column and eluted with methylene chloride to yield 2-bromo-4′-benyloxyacetophenone. An Rf of 0.62 was observed when resolved by thin layer chromatography using methylene chloride. 1H nmr (δ, ppm, CDCl3), 7.97 (2H, δ, 9.2 Hz, O—Ar—C(O)), 7.43 (5H, m, Ar′CH2O—), 7.04 (2H, δ, 9.0 Hz, O—Ar—C(O)), 5.15 (2H, s, Ar′CH2O—), 4.40 (2H, s, CH2 Br).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06916802B2
Source datasetuspto-grants-2005_07
ORD IDord-ee99d101054d4e76878ff79626deeb28
Source noteuspto-grants-2005_07