HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1180656Generated: October 27, 2026
Hydrochloric Acid → 5-Methylbenzo[b]thiophene-2-sulfonamide
https://huagongshe.com/reaction/1180656
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | 5-Methylbenzo(b)thiophene | HCID 84346 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 5-Methylbenzo[b]thiophene-2-sulfonamide | HCID 13922866 | 16% |
Reaction Steps
5-Methyl-benzo[b]thiophene (220 mg, 1.5 mmol) is dissolved in dry THF (1.5 mL) and cooled to 0° C. To this solution is slowly added 1.6 M n-BuLi in hexane (1.0 mL, 1.6 mmol) and the temperature maintained at 0° C. and the reaction mixture stirred for 20 min. Then the heterogeneous mixture is diluted with 2 mL of THF and transferred by canula to a well-stirred solution of sulfuryl chloride (245 μL, 4.6 mmol) in hexane (1.5 mL) at 0° C. After 1 hr, the suspension is diluted with acetone and the resulting solution of acid chloride is added slowly to a solution of 2 mL of NH4OH in acetone (5 mL). The mixture is diluted with water and acidified with conc. HCl. The aqueous solution is acidified and the product is extracted into ethyl acetate. The organic phase is washed with water and brine, dried (Na2SO4), and evaporated. The crude product is purified by silica gel chromatography (eluent: hexane 3/ethyl acetate 1) to afford the title compound (53 mg, 16%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07282595B2 |
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| Source dataset | uspto-grants-2007_10 |
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| ORD ID | ord-64e5204956f14aac8b1cc3bfa721080f |
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| Source note | uspto-grants-2007_10 |
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