HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1075268Generated: November 2, 2026
O-Methylhydroxylamine hydrochloride → HCID 54097963, compound
https://huagongshe.com/reaction/1075268
Participants
| Role | Name | HCID | Charge |
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| Reactant | O-Methylhydroxylamine hydrochloride | HCID 521874 | — |
| Reactant | HCID 23690652 | HCID 23690652 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 54097963 | HCID 54097963 | — |
Reaction Steps
To a solution of O-methylhydroxylamine hydrochloride (0.25 g.) in methanol (6 ml.) was added a mixture of potassium 2-(4-aminopyrimidin-2-yl)glyoxylate and its monohydrate with stirring at ambient temperature, and the mixture was stirred for 4 hours. The reaction mixture was allowed to stand overnight at ambient temperature, filtered, and the filtered precipitates were washed with ethanol. After the filtrate and washings were combined together, the solvents were distilled off. The resultant oily substance was pulverized in acetone (15 ml.) and collected by filtration. Thus obtained powder was washed successively with acetone and diethyl ether and then dried to give a pale brown powder of 2-(4-aminopyrimidin-2-yl)-2-methoxyiminoacetic acid (syn isomer) (290 mg.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04395411 |
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| Source dataset | uspto-grants-1983_07 |
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| ORD ID | ord-6e35c6bf512440eab153b19b89b14f0f |
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| Source note | uspto-grants-1983_07 |
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