HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537634Generated: October 26, 2026
Hydroxyamine hydrochloride → HCID 178464427, compound
https://huagongshe.com/reaction/537634
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | 4-(4-(Ethyl(2-hydroxyethyl)amino)phenyl)naphthalene-1,2-dione | HCID 49844959 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178464427 | HCID 178464427 | — |
Reaction Steps
A suspension of 4-(4-(ethyl(2-hydroxyethyl)amino)phenyl)naphthalene-1,2-dione (8.5 g, 26.48 mmol) in absolute ethanol (150 ml) was treated in one portion with hydroxylamine hydrochloride (3.68 g, 52.96 mmol) recrystallised from 75:25 EtOH:H2O and stirred at RT for 2 hrs. The mixture was then evaporated in vacuo and the residue suspended in H2O (500 ml). The aqueous phase was then basified to pH 10 with ammonium hydroxide solution and extracted into EtOAc (×4). The combined organics were then dried (Na2SO4) and evaporated in vacuo to afford the product, 4-(4-(ethyl(2-hydroxyethyl)amino)phenyl)-2-(hydroxyimino)naphthalen-1(2H)-one, as a dark red solid (9.1 g, 100%). Analysis of the product by 1H NMR gave a spectrum consistent with the structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08865029B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-7703511bee304673bb000e11d7eb6f9c |
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| Source note | uspto-grants-2014_10 |
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