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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 731352Generated: October 26, 2026

Cyclohexylamine → Ethyl 2-(Cyclohexylamino)cyclopentanecarboxylate

https://huagongshe.com/reaction/731352

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexylamineHCID 7965—
ReactantEthyl 2-oxocyclopentanecarboxylateHCID 69136—
ReactantSodium cyanoborohydrideHCID 5003444—
CatalystAcetic AcidHCID 176—
SolventEthanolHCID 702—
ProductEthyl 2-(Cyclohexylamino)cyclopentanecarboxylateHCID 5767118986.9%

Reaction Conditions

Temperature50 °C

Reaction Steps

A solution of 2-oxo-cyclopentanecarboxylic acid ethyl ester (2.01 g, 12.9 mmol) in ethanol (20 mL) was treated with cyclohexylamine (1.75 mL, 12.1 mmol), sodium cyanoborohydride (1.39 g, 22.2 mmol), and glacial acetic acid (10 drops) and stirred for 16 h at 50° C. After cooling to 25° C. the solvent was removed in vacuo, the crude material was redissolved in ethyl acetate (100 mL), washed with saturated aqueous sodium bicarbonate solution (100 mL). The aqueous layer was discarded and the organic layer was washed with 1.0 M aqueous hydrochloric acid solution (50 mL). The organic layer was discarded, 1.0 M aqueous sodium hydroxide solution (75 mL) was added and the aqueous layer was extracted with ethyl acetate (100 mL). The organic layer was dried over sodium sulfate, filtered and the solvent was removed in vacuo to afford the desired product 2-cyclohexylamino-cyclopentanecarboxylic acid ethyl ester (2.10 g, 8.77 mmol, 86.9%), as a light yellow oil. LC-MS (ESI) calcd for C14H25NO2239.19, found 240.2 [M+H+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582626B2
Source datasetuspto-grants-2009_09
ORD IDord-d926f78938894c88a63ffb817468f5e2
Source noteuspto-grants-2009_09