HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1246663Generated: October 30, 2026
O-Methylhydroxylamine → HCID 178502860, compound
https://huagongshe.com/reaction/1246663
Participants
| Role | Name | HCID | Charge |
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| Reactant | O-Methylhydroxylamine | HCID 4113 | — |
| Reactant | 4-(Azidomethyl)benzonitrile | HCID 11073691 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 178502860 | HCID 178502860 | — |
Reaction Steps
4-Azidomethylbenzonitrile (17.3 g, 0.109 mol; Nishiyama et al; Chem. Lett. (1982) 1477) was dissolved in 500 mL of toluene and 200 mL of absolute ethanol. The solution was cooled to −10° C. and HCl(g) was bubbled through until saturation. The mixture was kept in the refrigerator for 2 days when most of the solvents were evaporated. Diethyl ether was added and was decanted off. The product was re-dissolved in a solution of O-methylhydroxyl amine (10.5 g, 0.125 mol) and triethyl amine (56 mL) in 200 mL of methanol. The mixture was allowed to stand for 3 days whence the methanol was evaporated with addition of EtOAc. The organic phase was washed with water, dilute HOAc and aqueous sodium bicarbonate, dried (Na2SO4) and diluted with more EtOAc to a total volume of 500 mL.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07129233B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-4b62ca25a18445cca3f8bb71f4f5cd6b |
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| Source note | uspto-grants-2006_10 |
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