HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2064689Generated: October 31, 2026
Hydrochloric Acid → 4-amino-N-benzyl-3-nitrobenzene-1-sulfonamide
https://huagongshe.com/reaction/2064689
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | (4-Benzylsulfamoyl-2-nitro-phenyl)-carbamic acid ethyl ester | HCID 20784934 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-amino-N-benzyl-3-nitrobenzene-1-sulfonamide | HCID 22477651 | 83.1% |
Reaction Steps
To a stirred suspension of (4-Benzylsulfamoyl-2-nitro-phenyl)-carbamic acid ethyl ester (1.50 g, Reference Example 62) in ethanol (30 ml) was added 2M sodium hydroxide solution (5.93 ml) and the reaction heated at 75° C. for 2 hours. The reaction mixture was cooled to ambient temperature, poured onto ice-water and acidified to pH3 with 2M hydrochloric acid (30 ml). The resultant precipitate was collected by filtration and dried in vacuo to give 4-amino-N-benzyl-3-nitro-benzenesulfonamide (1.01 g) as a yellow solid. LC-MS (METHOD J): RT=3.41 minutes, 308.22 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08288425B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-7b5c0c37f2834f88a897e1c8c58e749a |
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| Source note | uspto-grants-2012_10 |
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