HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35279Generated: October 29, 2026
Hydroxyamine hydrochloride → 4-Phenoxyphenoxyacetone oxime
https://huagongshe.com/reaction/35279
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 4-Phenoxyphenoxyacetone | HCID 13771702 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Phenoxyphenoxyacetone oxime | HCID 86742365 | — |
Reaction Steps
Over about 1 hour, a solution of 22 g of hydroxylamine hydrochloride and 26 g of anhydrous sodium acetate in 110 ml of water is added dropwise at room temperature to a solution of 64 g of 4-phenoxyphenoxyacetone in 260 ml of ethanol. After the slightly exothermic reaction has subsided, the mixture is stirred for a further 3.5 hours at reflux temperature. Subsequently, the ethanol is distilled off from the reaction mixture by rotary evaporation, the aqueous residue is extracted three times with a 2:1 mixture of ether and hexane, the combined organic phases are washed with water and with 10% sodium bicarbonate solution and then dried over sodium sulfate. The solvent is then distilled off. Recrystallisation from a mixture of diethyl ether and pentane affords 4-phenoxyphenoxyacetone oxime with a melting point of 59°-61° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04766152 |
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| Source dataset | uspto-grants-1988_08 |
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| ORD ID | ord-f4cb6a7e299043e7b3155f8a624b2916 |
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| Source note | uspto-grants-1988_08 |
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