HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1393837Generated: October 31, 2026
Ethanol → N-[2-(4-aminophenylamino)ethyl]-N-methylmethanesulfonamide sulfate
https://huagongshe.com/reaction/1393837
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | N-methyl-N-[2-(4-nitrophenylamino)ethyl]methanesulfonamide | HCID 23104462 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Product | N-[2-(4-aminophenylamino)ethyl]-N-methylmethanesulfonamide sulfate | HCID 69204989 | — |
Reaction Steps
A mixture of zinc powder (25 g), ammonium chloride (1.1 g), water (11.2 mL), and 96% ethanol (67.5 mL) was brought to reflux in a boiling water bath. N-methyl-N-[2-(4-nitrophenylamino)ethyl]methanesulfonamide (23) (12.3 g, 0.045 mol) was added in portions and heating was continued until the reaction medium decolorized. The resulting mixture was filtered while boiling and the filtrate was recovered onto 3.8 mL of 96% sulfuric acid. The zinc was washed with ethanol, the filtrate was cooled in ice, and the precipitate that formed was filtered off by suction. After recrystallization from 30 mL of ethanol and 30 mL of water, 14.4 g of product were isolated. A second recrystallization from 45 mL of 50% ethanol gave 11.5 g of expected product having the following elemental analyses:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07347879B2 |
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| Source dataset | uspto-grants-2008_03 |
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| ORD ID | ord-195f2bf1945a41fe8795142af42ca395 |
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| Source note | uspto-grants-2008_03 |
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