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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1383563Generated: October 31, 2026

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

https://huagongshe.com/reaction/1383563

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

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, CH2Br).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06255336B1
Source datasetuspto-grants-2001_07
ORD IDord-cbe4c4e3701445d19b89f8cac9d65cd1
Source noteuspto-grants-2001_07