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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxylamineHCID 787—
ReactantWaterHCID 962—
Reactant5-({[t-Butyl(dimethyl)silyl]oxy}methyl)-3-furonitrileHCID 68522108—
SolventEthanolHCID 702—
SolventDiethyl EtherHCID 3283—
Product5-({[t-Butyl(dimethyl)silyl]oxy}methyl)-N'-hydroxyfuran-3-carboximidamideHCID 8662021097%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07687491B2
Source datasetuspto-grants-2010_03
ORD IDord-be3e4a1c91a14d39b2449544ee5a8503
Source noteuspto-grants-2010_03