HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1066338Generated: November 1, 2026
Water → N-(n-pentanesulfonyl)-3-amino-4-nitrobenzamide
https://huagongshe.com/reaction/1066338
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | N-(n-pentanesulfonyl)-3-(acetylamino)-4-nitrobenzamide | HCID 21198585 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-(n-pentanesulfonyl)-3-amino-4-nitrobenzamide | HCID 21198604 | — |
Reaction Steps
The above partially purified product of N-(n-pentanesulfonyl)-3-(acetylamino)-4-nitrobenzamide was mixed with 300 ml of water and 500 ml of ethanol. Two-hundred grams of a 10%-sodium hydroxide aqueous solution were added thereto, and the mixture was stirred at 45 to 50° C. for 6 hours. The solvent (approx. 300 ml) was evaporated under reduced pressure. The resulting residue was neutralized with 10% hydrochloric acid aqueous solution and adjusted to pH 2 with diluted hydrochloric acid. The precipitated crystals were collected by filtration and dried to give 85.0 g of yellow crystals of N-(n-pentanesulfonyl)-3-amino-4-nitrobenzamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06242474B1 |
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| Source dataset | uspto-grants-2001_06 |
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| ORD ID | ord-a720b1cead6a4e5ebdec248b4897d014 |
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| Source note | uspto-grants-2001_06 |
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