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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1088725Generated: November 4, 2026

Allyl bromide → HCID 14820506, compound

https://huagongshe.com/reaction/1088725

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantPotassium CarbonateHCID 11430—
ReactantBenzo[b]thiophene-5-ol, 2,3-dihydro-HCID 11367101—
SolventAcetoneHCID 180—
ProductHCID 14820506HCID 1482050683.4%

Reaction Steps

To a solution of 5-hydroxy-2,3-dihydrobenzothiophene (1.53 g, 10.05 mmoles) in 200 mL acetone was added K2CO3 (12.5 g, 90.45 mmoles) with good mechanical stirring. The suspension was warmed and allyl bromide (4.86 g, 40.20 mmoles) was added in one portion. The reaction mixture was then heated to reflux overnight. After cooling, the solids were removed by filtration and the filtrate concentrated. The residue was taken up in 50/50 vol/vol hexane/methylene chloride and refiltered to remove the remaining salts. Concentration afforded 3.2 q crude product (a yellow oil) which was purified by flash chromatography (3% EtOAc in hexane to elute) to give 1.61 g pure product (83.4%) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04963580
Source datasetuspto-grants-1990_10
ORD IDord-f0097dec01dd4648a6d02265a4057a28
Source noteuspto-grants-1990_10