HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2252052Generated: November 2, 2026
Hydrochloric Acid → Benzenesulfonamide, 4-(hydroxymethyl)-N-methyl-
https://huagongshe.com/reaction/2252052
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4-(Methylsulfamoyl)benzoic acid | HCID 506056 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Benzenesulfonamide, 4-(hydroxymethyl)-N-methyl- | HCID 17981768 | 75% |
Reaction Steps
Add methyl amine (4.5 mL, 2 M in dichloromethane) to a mixture of 4-chlorosulfonyl benzoic acid (0.5 g) and dichloromethane (20 mL). Stir at room temperature overnight. Quench by pouring the reaction mixture into a mixture of saturated aqueous ammonium chloride and ethyl acetate. Separate the layers, wash the organic phase with water, dry the remaining organic phase over sodium sulfate and then concentrate under reduced pressure to provide (0.40 g, 82%) of an oil. Add borane-tetrahydrofuran complex (7.44 mL, 1 M) to a mixture of 4-methylsulfamoyl-benzoic acid (0.4 g) and tetrahydrofuran (10 mL) at 0° C. Heat at 80° C. for 3 hours. Cool at room temperature and add 1 N aqueous hydrochloric acid (20 mL) and extract with ethyl acetate. Wash with saturated aqueous sodium bicarbonate and dry the remaining organic phase over sodium sulfate and concentrate under reduced pressure to provide (0.28 g, 75%) of an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07320995B2 |
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| Source dataset | uspto-grants-2008_01 |
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| ORD ID | ord-f707af3d727648f9a6a8a483e0334c30 |
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| Source note | uspto-grants-2008_01 |
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