HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1015707Generated: October 26, 2026
3-Cyanobenzene-1-sulfonyl chloride → 3-(Aminomethyl)-N,N-dimethylbenzenesulfonamide
https://huagongshe.com/reaction/1015707
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Cyanobenzene-1-sulfonyl chloride | HCID 2801360 | — |
| Reactant | Dimethylamine methanol | HCID 22497844 | — |
| Product | 3-(Aminomethyl)-N,N-dimethylbenzenesulfonamide | HCID 16795356 | — |
Reaction Steps
(Step 1) To a 2M dimethylamine methanol solution (3.7 ml) was added 3-cyanobenzenesulfonyl chloride (1.5 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 (0.79 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,N-dimethylbenzenesulfonamide (1.0 g) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07985862B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-7ca78532832642ad8afbc1ebc98956d5 |
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| Source note | uspto-grants-2011_07 |
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