HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 236525Generated: October 30, 2026
Chlorosuccinimide → 4-Methylthiophene-3-sulfonyl chloride
https://huagongshe.com/reaction/236525
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | Lithium 4-methyl-3-thiophenesulfinate | HCID 23669555 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 4-Methylthiophene-3-sulfonyl chloride | HCID 23261674 | — |
Reaction Steps
To 34 g of lithium 4-methyl-3-thiophenesulfinate in 220 ml of water cooled to 10° C. was added a suspension of 26.7 g of N-chlorosuccinimide in 80 ml of 2-propanol portionwise during 5 minutes. An additional 75 ml of 2-propanol was added to dissolve the reagents and the mixture was stirred for 70 minutes at 20° C. A large excess (1 liter) of water was then added and the mixture was extracted with methylene chloride 3 times. The methylene chloride portions were combined, dried over sodium sulfate and the solvent removed in vacuo to yield 4-methyl-3-thiophenesulfonyl chloride. This product was dissolved in 100 ml of tetrahydrofuran and 70 ml of concentrated aqueous ammonia was then added, and the mixture stirred overnight. Concentration of the resultant solution in vacuo and dilution of the residue with water yielded a solid which was filtered, washed with water and stirred with hot 1-chlorobutane, cooled and filtered to yield 14 g of the desired solid compound, m.p. 73°-85°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04645529 |
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| Source dataset | uspto-grants-1987_02 |
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| ORD ID | ord-2bc43389863440bda78fe01356a6c85f |
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| Source note | uspto-grants-1987_02 |
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