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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 38426Generated: October 25, 2026

Acetone → 2-Bromo-1-thiophen-3-yl-butan-1-one

https://huagongshe.com/reaction/38426

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
Reactanttert-ButanolHCID 6386—
Reactant2-Bromo-1-thiophen-3-yl-butan-1-oneHCID 59598618—
ReactantHCID 178461630HCID 178461630—
SolventBenzeneHCID 241—
Product2-Bromo-1-thiophen-3-yl-butan-1-oneHCID 59598618—
Product5-Thiophen-3-yl-heptane-2,4-dioneHCID 59598638—

Reaction Conditions

Temperature0 °C

Reaction Steps

EtMgBr (6.69 ml, 13 mmol, 2 M in ethyl ether) in benzene (10 ml) was cooled to zero degrees C., and tBuOH (1.28 ml, 13 mmol) was slowly added. The reaction mixture was stirred at zero degrees C. for 5 minutes, then acetone (530 ul, 7 mmol) was added, followed by a solution of 2-Bromo-1-thiophen-3-yl-butan-1-one (1.3 g, 6 mmol) in 3 ml benzene via cannula. The reaction mixture was heated to reflux for 1 hour, and acetone (250 ul) was added. The reaction mixture was heated 2 hours more at reflux. The reaction was cooled, quenched with 1 N HCl (10 ml), extracted three times with diethyl ether, washed brine, and dried over magnesium sulfate. The solvent was removed in vacuo and the residue chromatographed (5% ethyl acetate/hexanes) to give 247 mg of 2-Bromo-1-thiophen-3-yl-butan-1-one starting material and 520 mg of 5-Thiophen-3-yl-heptane-2,4-dione, 44%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524725B2
Source datasetuspto-grants-2013_09
ORD IDord-bc19b9a175a54cfebeeaa16f982df689
Source noteuspto-grants-2013_09