HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 26799Generated: October 29, 2026
Hydroxyamine hydrochloride → Propanediamide, N,N-diphenyl-N'-hydroxy-2-methyl-
https://huagongshe.com/reaction/26799
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | HCID 23339622 | HCID 23339622 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Propanediamide, N,N-diphenyl-N'-hydroxy-2-methyl- | HCID 3049613 | 68% |
Reaction Steps
4.9 g (0.125 gram atom) of sodium in small pieces are added to 50 ml of anhydrous methanol and 2/3 of the sodium ethylate solution thus obtained is used to neutralise a solution of 5.25 g (0.075 mol) of hydroxylamine hydrochloride in 50 ml of anhydrous methanol; 15 g (0.05 mol) of ethyl 2-(N,N-diphenylcarbamoyl)-propionate are then added, after which the remaining one-third of the sodium ethylate solution is added in the cold. The reactants are left in contact overnight at 50° C., the mixture is evaporated to dryness in vacuo, the residue is taken up in ether and the sodium salt is filtered off, dissolved in water and acidified with concentrated HCl. CRL 40,438 is obtained by filtering off, drying and recrystallising from acetonitrile. Melting point: 171°-172° C. Yield: 68%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04151300 |
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| Source dataset | uspto-grants-1979_04 |
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| ORD ID | ord-79b6520e19a64bea91ae428a522f7756 |
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| Source note | uspto-grants-1979_04 |
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