HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 647561Generated: October 31, 2026
Hydroxyamine hydrochloride → HCID 54186551, compound
https://huagongshe.com/reaction/647561
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | Potassium Bicarbonate | HCID 516893 | — |
| Reactant | HCID 13092564 | HCID 13092564 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Solvent | Water | HCID 962 | — |
| Product | Hydroxylamine | HCID 787 | — |
| Product | HCID 54186551 | HCID 54186551 | 86.1% |
Reaction Steps
An aqueous solution of hydroxylamine is prepared from 39.06 g (0.562 mol) of hydroxylamine hydrochloride in 150 ml of water and from 56.2 g (0.562 mol) of potassium bicarbonate. 48.9 g (0.225 mol) of 4-(o-allylphenoxy)-3-hydroxy-butyronitrile previously dissolved in 250 ml of n-butanol are then added. The resulting mixture is taken to 80° C. in about 2 hours, then taken to reflux (94° C.) which is maintained for 5 hours. The mixture is cooled, the H2O--CH3 (CH2)2CH2OH mixture is evaporated, the residue of evaporation is taken up with ether, washed several times in water, dried and the ether is evaporated under reduced pressure. 48.5 g (yield 86%) of 4-(o-allyl-phenoxy)-3-hydroxy-butyramidoxime are obtained in the form of a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04409242 |
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| Source dataset | uspto-grants-1983_10 |
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| ORD ID | ord-6a8d6b930d8a4a289bc2418be4ae15d7 |
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| Source note | uspto-grants-1983_10 |
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