HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1906374Generated: October 31, 2026
4-Nitrobenzenesulfonyl chloride → N-(Cyanomethyl)-4-nitrobenzenesulfonamide
https://huagongshe.com/reaction/1906374
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Nitrobenzenesulfonyl chloride | HCID 7404 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Aminoacetonitrile hydrochloride | HCID 11491918 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-(Cyanomethyl)-4-nitrobenzenesulfonamide | HCID 3113405 | 72.5% |
Reaction Steps
To a stirred solution of 27.8 g (0.3 moles) aminoacetonitrile hydrochloride in 200 ml water, 24 g (0.3 moles) sodium hydroxide (50% aqueous) were added. The resulting mixture was cooled to about 20° C. with an ice bath. The ice bath was removed; then 22.2 g (0.1 mole) 4-nitrobenzenesulfonyl chloride were added. The reaction mixture was stirred 18 hours at ambient temperature. The solids were filtered. The resulting wet cake was crystallized from 50 ml ethanol. The solids were dried in vacuo to give 17.5 g of the above-identified product as a dark-yellow solid, melting point 115°-120° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04652556 |
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| Source dataset | uspto-grants-1987_03 |
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| ORD ID | ord-b177908c9c3942a5b0e4ec6a6f7c9ae2 |
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| Source note | uspto-grants-1987_03 |
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