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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1621225Generated: November 3, 2026

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

https://huagongshe.com/reaction/1621225

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 numberUS08772507B2
Source datasetuspto-grants-2014_07
ORD IDord-36cc8a6f4da84e78b7fc35b4c9a63787
Source noteuspto-grants-2014_07