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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2260123Generated: October 31, 2026

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

https://huagongshe.com/reaction/2260123

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzo(B)ThiopheneHCID 7221—
ReactantBromineHCID 24408—
Reactant4-[(Benzo[b]thiophene-3-yl)carbonyl]-1-piperidinecarboxylic acid, 1,1-dimethylethyl esterHCID 15337456—
SolventCarbon TetrachlorideHCID 5943—
ProductBenzo(b)thiophene, 3-bromo-HCID 12325048%

Reaction Steps

4-[(Benzo[b]thiophene-3-yl)carbonyl]-1-piperidinecarboxylic acid, 1,1-dimethylethyl ester ##STR13## 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 numberUS05476861
Source datasetuspto-grants-1995_12
ORD IDord-8ea860528bc2449592281ceddc95dc08
Source noteuspto-grants-1995_12