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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1491677Generated: October 30, 2026

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

https://huagongshe.com/reaction/1491677

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzo(B)ThiopheneHCID 7221—
ReactantBromineHCID 24408—
SolventCarbon TetrachlorideHCID 5943—
ProductBenzo(b)thiophene, 3-bromo-HCID 12325048.4%

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 numberUS05371093
Source datasetuspto-grants-1994_12
ORD IDord-503adf4606634cd59780046c6434c8ff
Source noteuspto-grants-1994_12