Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 62657Generated: October 30, 2026

2-Aminocyclohex-1-ene-1-carbonitrile → 2-aminocyclohexane-1-carbonitrile

https://huagongshe.com/reaction/62657

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Aminocyclohex-1-ene-1-carbonitrileHCID 290175—
ReactantSodium cyanoborohydrideHCID 5003444—
CatalystAcetic AcidHCID 176—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
Product2-aminocyclohexane-1-carbonitrileHCID 2116386378.6%

Reaction Steps

To a cold solution of 2-aminocyclohex-1-enecarbonitrile (I-7a: 50 mg, 0.41 mmol) in methanol (3 mL) was added NaCNBH3 (103 mg, 1.64 mmol) and acetic acid (5 drops) at 0° C. The resulting mixture was stirred at room temperature for 16h. The reaction mixture was diluted with ethyl acetate and the organic layer was washed with saturated NaHCO3, brine, dried over anhydrous Na2SO4 and concentrated to afford 40 mg (78%) of diastereomeric mixture of 2-aminocyclohexanecarbonitrile (I-7b) as a gum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09447039B2
Source datasetuspto-grants-2016_09
ORD IDord-362529fe20684a55b771015a2944a1df
Source noteuspto-grants-2016_09