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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1392731Generated: November 4, 2026

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

https://huagongshe.com/reaction/1392731

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-(tert-Butoxycarbonyloxyimino)-2-phenylacetonitrileHCID 93865—
ReactantCyclopentane-1,2-diamineHCID 243938—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
Productrac-tert-butyl N-((1R,2R)-2-aminocyclopentyl)carbamateHCID 1704021798.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

(±)-trans-1,2-Cyclopentanediamine (WO98/30574) (692 mg) was dissolved in methylene chloride (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 aqueous solution of sodium chloride and dried over anhydrous sodium sulfate. The residue was purified by flash column chromatography on silica gel (methylene chloride:methanol=9:1) to obtain the title compound (395 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07342014B2
Source datasetuspto-grants-2008_03
ORD IDord-d7b5c3f55cfc4acd874224a669e9dfb8
Source noteuspto-grants-2008_03