HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1069198Generated: October 29, 2026
O-Methylhydroxylamine hydrochloride → HCID 54031622, compound
https://huagongshe.com/reaction/1069198
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | O-Methylhydroxylamine hydrochloride | HCID 521874 | — |
| Reactant | Methyl 2-benzyloxyiminoacetoacetate | HCID 53919435 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 54031622 | HCID 54031622 | 91% |
Reaction Steps
To a solution of 4.0 g (17 mol) of methyl 2-benzyloxyiminoacetoacetate in 50 ml of methanol, 1.56 g (18.7 mmol) of methoxyamine hydrochloride was added and the mixture was heated under reflux for 3 hours. After distilling the solvent off under reduced pressure, 50 ml of water was added and the mixture was extracted twice with 50 ml of diethylether and then washed with water and a saturated aqueous sodium chloride. The organic layer was dried over with anhydrous magnesium sulfate and the solvent was distilled off to obtain a residue, which was then purified by a column chromatography on a silica gel (n-hexane/ethyl acetate) to obtain 4.11 g (yield:91%) of methyl 2-benzyloxyimino-3-methoxyiminobutyrate as a colorless oil. 1H-NMR(CDCl3) δ ppm:1.99(3H, s), 3.86(3H, s), 3.94(3H, s), 5.21(2H, s), 7.33(5H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06251949B1 |
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| Source dataset | uspto-grants-2001_06 |
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| ORD ID | ord-477e12dfda904a4fb099a61a894d883e |
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| Source note | uspto-grants-2001_06 |
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