HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2082890Generated: October 31, 2026
Water → 5-(Aminomethyl)-3-(butylamino)-2-phenoxybenzene-1-sulfonamide
https://huagongshe.com/reaction/2082890
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | 3-(Butylamino)-5-cyano-2-phenoxybenzene-1-sulfonamide | HCID 53898140 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 5-(Aminomethyl)-3-(butylamino)-2-phenoxybenzene-1-sulfonamide | HCID 54039296 | — |
Reaction Steps
To a stirred mixture of lithium aluminum hydride (5.0 g) and 1,2-dimethoxyethane (100 ml) a solution of 3-n-butylamino-4-phenoxy-5-sulfamylbenzonitrile (15 g) in dry 1,2-dimethoxyethane (150 ml) is during about 1 hour at 100° C. dropwise added, and the mixture is stirred and refluxed for a further 16 hours. After cooling, ethyl acetate (10 ml) followed by water (20 ml) are very cautiously added dropwise, whereafter the mixture is stirred for a further 30 minutes. It is then heated on a steam-bath and filtered hot; the filter-cake is carefully washed with hot 2-methoxyethanol (3 portions of 50 ml). The combined filtrates are evaporated in vacuo to yield crude 3-n-butylamino-4-phenoxy-5-sulfamylbenzylamine. After recrystallization from 2-methoxyethanol it is obtained with a melting point of 197°-198° C. The material (IR, analysis) is identical with the material prepared as in Example 289.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04082851 |
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| Source dataset | uspto-grants-1978_04 |
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| ORD ID | ord-aa2878dd7a734d3db809c5c1f4f2bb61 |
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| Source note | uspto-grants-1978_04 |
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