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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1714561Generated: November 2, 2026

Bromine → 2-Bromo-1-(4-iodophenyl)ethanone

https://huagongshe.com/reaction/1714561

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
Reactant1-(4-Iodophenyl)ethan-1-oneHCID 72869—
Solvent1,4-DioxaneHCID 31275—
Product2-Bromo-1-(4-iodophenyl)ethanoneHCID 256572—

Reaction Steps

A solution of 1-(4-iodophenyl)ethanone (55.9 mmol) in dioxane (160 mL) was cooled to 10° C. Bromine (1.1 equiv, 61.6 mmol) was added dropwise to the reaction mixture. After 10 min, the cooling bath was removed and the reaction mixture was stirred at room temperature. After 1.5 h, the reaction mixture was concentrated in vacuo, poured into water (100 mL), and extracted with (3×100 mL) ethyl acetate. The combined organic layers were dried over sodium sulfate and concentrated in vacuo to a tan solid (18.2 g) which was used directly in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07795448B2
Source datasetuspto-grants-2010_09
ORD IDord-17492d2c7cf34194aab83ef7cbb032b1
Source noteuspto-grants-2010_09