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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1450421Generated: October 28, 2026

Benzo(B)Thiophene → Benzo(b)thiophene, 3-bromo-

https://huagongshe.com/reaction/1450421

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzo(B)ThiopheneHCID 7221—
ReactantBromineHCID 24408—
SolventCarbon TetrachlorideHCID 5943—
ProductBenzo(b)thiophene, 3-bromo-HCID 12325048,408%

Reaction Steps

Dissolve benzo[b]thiophene (23 g, 0.170 mmol) in carbon tetrachloride (80 mL). Add, by dropwise addition, a solution of bromine (26.85 g, 0.168 mmol) in carbon tetrachloride (30 mL) and stir at room temperature for 2 days. Quench with a 1M solution of sodium thiosulfate and separate the organic phase. Extract the aqueous phase with carbon tetrachloride, combine the organic phases and dry (MgSO4). Evaporate the solvent in vacuo and purify by distillation to give 3-bromobenzo[b]thiophene as a pale yellow liquid (17.33 g, 48%); bp 64°-72° C. @ 0.02 mm Hg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05602147
Source datasetuspto-grants-1997_02
ORD IDord-234bddfd26954db89cefe78f93d57cb9
Source noteuspto-grants-1997_02