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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 589664Generated: October 30, 2026

Chlorosulfonic acid → 5-bromo-3-methyl-1-benzothiophene-2-sulfonyl chloride

https://huagongshe.com/reaction/589664

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosulfonic acidHCID 24638—
Reactant5-Bromo-3-methyl-1-benzothiopheneHCID 14175764—
SolventChloroformHCID 6212—
Product5-bromo-3-methyl-1-benzothiophene-2-sulfonyl chlorideHCID 273559115,820.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

Chlorosulfonic acid (2.20 ml, 0.033 mmol) was added dropwise at −5° C. to a solution of 5-bromo-3-methylbenzothiophene (Intermediate 9) (3.0 g, 13.2 mmol) in CHCl3 (30 mL). The reaction mixture was stirred at 0° C. for 3 h, and then poured into a mixture of ice/NaHCO3 and stirred vigorously for 5 min. The organic phase was immediately separated, dried and concentrated to give the title compound (1.70 g, 39%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09233946B2
Source datasetuspto-grants-2016_01
ORD IDord-39d18a88475e4d4299d79ad7130e426a
Source noteuspto-grants-2016_01