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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1662052Generated: October 30, 2026

Water → HCID 86644626, compound

https://huagongshe.com/reaction/1662052

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantHCID 59454078HCID 59454078—
SolventEthanolHCID 702—
ProductHCID 86644626HCID 8664462665.6%

Reaction Conditions

Temperature70 °C

Reaction Steps

tert-Butyl [(1S,2R)-2-cyanocyclopentyl]carbamate (415 mg) and hydrochloric acid hydroxylamine (411 mg) were suspended in ethanol (6.2 ml), triethylamine (0.83 ml) was added thereto at room temperature, and the reaction mixture was then stirred at 70° C. for 24 hours. The reaction mixture was left to be cooled, and hydrochloric acid hydroxylamine (411 mg) and triethylamine (0.83 ml) were added thereto, followed by stirring at 75° C. for an additional 48 hours. The reaction mixture was left to be cooled, and water (30 ml) was added thereto, followed by extraction with ethyl acetate (40 ml). The organic layer was washed with a saturated sodium bicarbonate solution and saturated brine in this order and dried over anhydrous magnesium sulfate. The solvent was then removed by evaporation under reduced pressure. The residue was purified by silica gel column chromatography (1.5% methanol-chloroform) to obtain tert-butyl {(1S,2R)-2-[amino(hydroxyimino)methyl]cyclopentyl}carbamate (315 mg) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030489B2
Source datasetuspto-grants-2011_10
ORD IDord-6aa1855ccd754a4db46ce5f3f578de6c
Source noteuspto-grants-2011_10