HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2164364Generated: October 31, 2026
Hydroxylamine, O-ethyl- → HCID 136399315, compound
https://huagongshe.com/reaction/2164364
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydroxylamine, O-ethyl- | HCID 69357 | — |
| Reactant | HCID 178458867 | HCID 178458867 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 136399315 | HCID 136399315 | — |
Reaction Steps
Into 10 ml of tetrahydrofuran was dissolved 2.0 g of 5-(4-acetamidophenyl)-2-propionyl-3-hydroxy-2-cyclohexen-1-one and to the solution was added 1.0 g of aqueous solution containing 50% of ethoxyamine. The mixture was kept for 15 hours at room temperature and it was poured into ice water and the crystal sedimented was collected with a filtering step. The crystal was dissolved in 20 ml of chloroform and the solution was washed with water and extracted with 15 ml of aqueous solution containing 5% of sodium hydroxide. To the alkaline solution was added a dilute hydrochloric acid solution and the crystal sedimented was extracted with chloroform. The solution was washed with water and dried with anhydrous magnesium sulfate and the chloroform was distilled off from it under reduced pressure. Thus 1.4 g of the desired compound was obtained. It was in the form of pale yellow crystals having a melting point of 135°-136° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04504305 |
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| Source dataset | uspto-grants-1985_03 |
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| ORD ID | ord-6a88e8ebe1be482890d60694de37306f |
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| Source note | uspto-grants-1985_03 |
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