HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2247635Generated: October 26, 2026
Hydroxylamine → 5-({[t-Butyl(dimethyl)silyl]oxy}methyl)-N'-hydroxyfuran-3-carboximidamide
https://huagongshe.com/reaction/2247635
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydroxylamine | HCID 787 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 5-({[t-Butyl(dimethyl)silyl]oxy}methyl)-3-furonitrile | HCID 68522108 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 5-({[t-Butyl(dimethyl)silyl]oxy}methyl)-N'-hydroxyfuran-3-carboximidamide | HCID 86620210 | 97% |
Reaction Steps
To a solution of 5-({[t-butyl(dimethyl)silyl]oxy}methyl)-3-furonitrile (1.8 g, 7.6 mmol) that was obtained in Example 1 (1c) in ethanol (10 ml) was added a 40% aqueous solution of hydroxylamine (1.0 ml) with stirring, and the resulting mixture was stirred at 60° C. for 1 hour. After evaporating the reaction mixture in vacuo, the residue obtained was diluted with ether, poured into water (40 ml) and extracted with ether. The extract was washed with a saturated aqueous solution of sodium chloride and dried over magnesium sulfate. After filtration, the filtrate was evaporated in vacuo, and the crude product of the title compound thus obtained was purified by chromatography on a silica gel column using a mixed solvent of ethyl acetate and hexane (1:1) as the eluent to afford the title compound (2.0 g) in a yield of 97% as a white crystalline solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07687491B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-be3e4a1c91a14d39b2449544ee5a8503 |
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| Source note | uspto-grants-2010_03 |
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