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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2248960Generated: November 2, 2026

1-(Thiophen-3-yl)ethanone → 2-Bromo-1-(thiophen-3-yl)ethan-1-one

https://huagongshe.com/reaction/2248960

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Thiophen-3-yl)ethanoneHCID 15116—
ReactantBromineHCID 24408—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventDiethyl EtherHCID 3283—
Product2-Bromo-1-(thiophen-3-yl)ethan-1-oneHCID 277637985.4%

Reaction Steps

3-Acetylthiophene (6.3 g, 50 mmol) was dissolved in anhydrous ether (100 ml) and aluminium chloride (catalytic amount) added. Bromine (2.55 ml, 50 mmol) was added dropwise and then stirred for 10 min. The ether was removed under reduced pressure and the residue washed with water. The crude product was recrystallised from petroleum-ether (60°-80° C.) to yield 3-bromoacetylthiophene m.p. 54°-56° C. (8.76 g, 85%), δH (CDCl3) 8.15(1H, dd, H2), 7.55(1H, dd, H4'), 7.35(1H, dd, H5').

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05041567
Source datasetuspto-grants-1991_08
ORD IDord-80798c9ad9b94d61a032fecf18f227c2
Source noteuspto-grants-1991_08