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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 459464Generated: October 30, 2026

Water → rac-tert-butyl N-((1R,2S)-2-aminocyclopentyl)carbamate

https://huagongshe.com/reaction/459464

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-(tert-Butoxycarbonyloxyimino)-2-phenylacetonitrileHCID 93865—
Reactantcis-Cyclopentane-1,2-diamineHCID 11412654—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
Productrac-tert-butyl N-((1R,2S)-2-aminocyclopentyl)carbamateHCID 1844285698.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

cis-1,2-Cyclopentanediamine (WO98/30574) (692 mg) was dissolved in dichloromethane (10 ml), to which triethylamine (1.1 ml) and 2-(tert-butoxycarbonyloxy-imino)-2-phenylacetonitrile (493 mg) were added, and the mixture was stirred at 0° C. for 1 hour. Thereafter, 2-(tert-butoxycarbonyloxyimino)-2-phenylacetonitrile (493 mg) were additionally added, and the mixture was stirred at room temperature for 7 hours. Water was added to the reaction mixture to separate an organic layer. The organic layer was washed with saturated saline and dried over anhydrous sodium sulfate. The residue was purified by flash column chromatography on silica gel (dichloromethane:methanol=9:1) to obtain the title compound (395 mg) as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07192968B2
Source datasetuspto-grants-2007_03
ORD IDord-86a969cc765b49d8bb6e17065d1e0da5
Source noteuspto-grants-2007_03