HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 8633Generated: October 23, 2026
Dichloromethane → 2,5-Dichloro-4-methylthiophene-3-sulfonyl chloride
https://huagongshe.com/en/reaction/8633
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 3-Methylthiophene | HCID 12024 | — |
| Reactant | Chlorosulfonic acid | HCID 24638 | — |
| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Product | 2,5-Dichloro-4-methylthiophene-3-sulfonyl chloride | HCID 21983796 | 25% |
Reaction Steps
To a cooled (10° C.) solution of 3-methylthiophene (5 g, 50 mmol) in dichloromethane (15 mL) was added a solution of sulfuryl chloride (8.6 mL) in dichloromethane (5 mL). The reaction mixture was maintained at 10° C. for 30 minutes, then at ambient temperature for 16 hours. The reaction was concentrated and redissolved in dichloromethane (30 mL) and cooled to −10° C. To the cooled solution was added chlorosulfonic acid (2 mL, 100 mmol). The reaction was maintained at −10° C. for 30 minutes, then at ambient temperature for 16 hours, at which time it was poured into ice water (50 mL) and extracted with dichloromethane (50 mL). The organic layer was dried (Mg2SO4) and concentrated to furnish a brown oil (3.3 g, 25%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07091204B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-d3a94c6cd2a949a99cb74eb9ff971a3b |
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| Source note | uspto-grants-2006_08 |
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