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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 234700Generated: October 30, 2026

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

https://huagongshe.com/reaction/234700

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 (23g, 0.170mmol) in carbon tetrachloride (80mL). Add, by dropwise addition, a solution of bromine (26.85g, 0.168mmol) in carbon tetrachloride (30mL) 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 (17.33g, 48%); bp 64°-72° [email protected] Hg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05596003
Source datasetuspto-grants-1997_01
ORD IDord-ca2f65c1f4c94ef4be57b86f7d77fe73
Source noteuspto-grants-1997_01