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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2270601Generated: October 28, 2026

Sulfuryl chloride → 2-Methyl-1-benzothiophene-3-sulfonyl chloride

https://huagongshe.com/reaction/2270601

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuryl chlorideHCID 24648—
Reactant2-Methylbenzo(b)thiopheneHCID 70952—
SolventDimethylformamideHCID 6228—
Product2-Methyl-1-benzothiophene-3-sulfonyl chlorideHCID 22998449640%

Reaction Conditions

Temperature0 °C

Reaction Steps

Sulfuryl chloride (9.5 mmoles, 0.76 ml) was added to a stirred solution of dimethylformamide (DMF; 11.2 mmoles, 0.87 ml) at 0° C., and the resulting faint yellow solution was stirred for 20 min at 0° C. 2-Methylbenzo[b]thiophene (5.6 mmoles, 0.83 g) was then added, the reaction mixture was diluted with 2 ml of DMF, and then heated to 85° C. After 2.5 hrs at 85° C., the brown reaction mixture was cooled to ambient temperature and added to ice (100 ml). The aqueous phase was extracted with ethyl acetate (100 ml), and the organic phase was dried (MgSO4), filtered and concentrated to collect an orange-brown solid. Flash chromatography (4% ethyl acetate/hexanes) provided 0.89 g (640%) of 2-methylbenzo[b]thiophene-3-sulfonyl chloride as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06331637B1
Source datasetuspto-grants-2001_12
ORD IDord-26959f2714b345f7ac1c6b0d4f63cc8c
Source noteuspto-grants-2001_12