HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 447806Generated: October 26, 2026
3-Cyanobenzene-1-sulfonyl chloride → 3-(aminomethyl)-N-methylbenzenesulfonamide
https://huagongshe.com/reaction/447806
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Cyanobenzene-1-sulfonyl chloride | HCID 2801360 | — |
| Reactant | Monomethylamine methanol | HCID 57454252 | — |
| Product | 3-(aminomethyl)-N-methylbenzenesulfonamide | HCID 16785597 | — |
Reaction Steps
(Step 1) To a 40% methylamine methanol solution (5 ml) was added 3-cyanobenzenesulfonyl chloride (0.88 g) at 0° C., and the mixture was stirred at room temperature for 2 hr. The solvent was evaporated under reduced pressure, saturated brine was added, and the mixture was extracted with ethyl acetate. The solvent was evaporated under reduced pressure. 10% Palladium carbon powder (0.46 g) was added to a solution (10 ml) of the residue in ethanol, and the mixture was stirred overnight under a hydrogen atmosphere (1 atm). The solution was filtered through celite. The solvent was evaporated under reduced pressure. The residue was purified by basic silica gel column chromatography (ethyl acetate) to give 3-(aminomethyl)-N-methylbenzenesulfonamide (0.38 g) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08481569B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-e5c5022396b5479c9d25ae99dea3002b |
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| Source note | uspto-grants-2013_07 |
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