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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 2-(tert-Butoxycarbonyloxyimino)-2-phenylacetonitrile | HCID 93865 | — |
| Reactant | cis-Cyclopentane-1,2-diamine | HCID 11412654 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | rac-tert-butyl N-((1R,2S)-2-aminocyclopentyl)carbamate | HCID 18442856 | 98.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07192968B2 |
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| Source dataset | uspto-grants-2007_03 |
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| ORD ID | ord-86a969cc765b49d8bb6e17065d1e0da5 |
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| Source note | uspto-grants-2007_03 |
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