HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2361569Generated: October 31, 2026
Hydroxyamine hydrochloride → HCID 86644089, compound
https://huagongshe.com/reaction/2361569
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 59440843 | HCID 59440843 | — |
| Reactant | HCID 59440846 | HCID 59440846 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Water ethanol | HCID 19096565 | — |
| Product | HCID 86644089 | HCID 86644089 | — |
| Product | HCID 86644090 | HCID 86644090 | — |
Reaction Steps
A solution of a mixture of 4-methyl-1-vinyl-cyclohex-3-enecarbaldehyde and 3-methyl-1-vinyl-cyclohex-3-ene-carbaldehyde (6:4, 1.5 g, 10 mmol), hydroxylamine hydrochloride (1.04 g, 15 mmol) and NaHCO3 (1.26 g, 15 mmol) in EtOH/Water (20 ml, 3:1) was stirred at 50° C. for 4 h. The mixture was diluted with water and extracted 3 times with MTBE. The combined org. layers were washed with water and brine, dried (MgSO4) and evaporated in vacuo. 4-Methyl-1-vinyl-cyclohex-3-enecarbaldehyde oxime and 3-methyl-1-vinyl-cyclohex-3-ene-carbaldehyde oxime was obtained after bulb-to-bulb distillation (ratio 6:4, yield 70%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08691746B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-b4b9d3ad36d646e7820c8d1e707f5c0e |
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| Source note | uspto-grants-2014_04 |
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