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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2390958Generated: October 31, 2026

p-Toluenesulfonic acid monohydrate → 5-Bromo-1-benzothiophene

https://huagongshe.com/reaction/2390958

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantHCID 57615036HCID 57615036—
SolventAcetoneHCID 180—
Product5-Bromo-1-benzothiopheneHCID 277657896.9%

Reaction Steps

To acetone (600 mL) solution of 300 g of 5-bromo-2,3-dihydro-1-benzothiophen-3-ol was added 12.4 g of p-toluenesulfonic acid monohydrate, which was then refluxed for 2 hours. To the reaction solution was added 15.0 g of activated carbon, which was then stirred. Insoluble matter was filtered off and washed with 300 mL of acetone. The filtrate and washings were combined, to which was dropwise added 2700 mL of water at 5 to 15° C. The precipitate was collected by filtration to provide 268 g of 5-bromo-1-benzothiophene as pale purple solid form.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273902B2
Source datasetuspto-grants-2012_09
ORD IDord-a64c1fb1562e4e2184a5ef6478f9c063
Source noteuspto-grants-2012_09