Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 731360Generated: October 27, 2026

Cyclohexanone → 2-Cyclohexylamino-cyclohexanecarboxylic acid ethyl ester

https://huagongshe.com/reaction/731360

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexanoneHCID 7967—
ReactantSodium BicarbonateHCID 516892—
Reactantethyl (1R,2S)-2-aminocyclohexane-1-carboxylate hydrochlorideHCID 2724641—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
Product2-Cyclohexylamino-cyclohexanecarboxylic acid ethyl esterHCID 5767121662.4%

Reaction Conditions

Temperature25 °C

Reaction Steps

cis-2-Amino-cyclohexanecarboxylic acid ethyl ester hydrochloride (0.5 g, 2.407 mmol) was dissolved in methanol (25 mL). Cyclohexanone (0.236 g, 2.407 mmol) was added followed by acetic acid (0.1 mL). The solution was stirred at 25° C. for 10 min. Sodium cyanoborohydride (0.378 g, 6.018 mmol) was added and the mixture was stirred at 25° C. for 16 h. The mixture was poured into 1/2 saturated aqueous sodium bicarbonate solution (300 mL). The aqueous layer was extracted with ethyl acetate (3×100 mL). The combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo to afford the crude product, 2-cyclohexylamino-cyclohexanecarboxylic acid ethyl ester (0.38 g, 1.5 mmol, 62.4%), as a clear oil. LC-MS (ESI) calcd for C15H27NO2 253.20, found 253.9 [M+H+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582626B2
Source datasetuspto-grants-2009_09
ORD IDord-8141e6160912452bb37b650d759f19b1
Source noteuspto-grants-2009_09