HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2209677Generated: October 31, 2026
Hydroxyamine hydrochloride → N-hydroxy-2-[[4-methoxybenzenesulfonyl](benzyl)amino]propionamide
https://huagongshe.com/reaction/2209677
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | Methyl 2-[[4-methoxybenzenesulfonyl](benzyl)amino]propionate | HCID 22907154 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-hydroxy-2-[[4-methoxybenzenesulfonyl](benzyl)amino]propionamide | HCID 15296597 | — |
Reaction Steps
Methyl 2-[[4-methoxybenzenesulfonyl](benzyl)amino]propionate (2.1 g, 6.01 mmol) is dissolved in methanol (20.0 mL). To this solution is added hydroxylamine hydrochloride (0.84 g, 12.0 mmol), followed by the addition of sodium methoxide (7.0 mL of a 4.37M solution). The reaction is stirred overnight at room temperature. The reaction is worked up by first removing all the solvent, and partitioning between ethyl acetate/hexane (2/1) and saturated sodium bicarbonate. The aqueous phase is extracted well with ethyl acetate/hexane, the combined organic layers are dried (MgSO4), and the solvent is evaporated. The product is purified by silica gel chromatography (ethyl acetate) to give N-hydroxy-2-[[4-methoxybenzenesulfonyl](benzyl)amino]propionamide, m.p. 149°-151° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05455258 |
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| Source dataset | uspto-grants-1995_10 |
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| ORD ID | ord-38e21aeeba7540168582deef9e506322 |
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| Source note | uspto-grants-1995_10 |
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