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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | 2-Methylbenzo(b)thiophene | HCID 70952 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Methyl-1-benzothiophene-3-sulfonyl chloride | HCID 22998449 | 640% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06331637B1 |
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| Source dataset | uspto-grants-2001_12 |
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| ORD ID | ord-26959f2714b345f7ac1c6b0d4f63cc8c |
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| Source note | uspto-grants-2001_12 |
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