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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2220006Generated: October 29, 2026

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

https://huagongshe.com/reaction/2220006

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzo(B)ThiopheneHCID 7221—
ReactantBromineHCID 24408—
SolventChloroformHCID 6212—
ProductBenzo(b)thiophene, 3-bromo-HCID 12325085.3%

Reaction Steps

A mixture of 6 g (0.044 mol) of Benzo[b]thiophene and 80 mL of CHCl3. is cooled by using an ice-water bath. A solution of 7.89 g (0.044 mol) of Br2 and 40 mL of CHCl3 is added slowly. After the addition is completed, the mixture is stirred for 1 h at room temperature and then hydrolysed with 150 mL of saturated aqueous Na2S2O6 solution. The aqueous phase is extracted two times with 150 mL of CHCl3. The combined organic phases are washed several times with water, dried over magnesium sulfate and then are concentrated under reduced pressure. The crude product is purified by distillation to give a colourless liquid (8.0 g, 84% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07416682B2
Source datasetuspto-grants-2008_08
ORD IDord-e55916e356a54d61890a959e215ead5d
Source noteuspto-grants-2008_08