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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 731258Generated: November 2, 2026

Cyclopentylamine → HCID 57671231, compound

https://huagongshe.com/reaction/731258

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopentylamineHCID 2906—
ReactantEthyl 2-oxocyclopentanecarboxylateHCID 69136—
ReactantSodium cyanoborohydrideHCID 5003444—
CatalystAcetic AcidHCID 176—
SolventEthanolHCID 702—
ProductHCID 57671231HCID 5767123134.2%

Reaction Conditions

Temperature50 °C

Reaction Steps

A solution of 2-oxo-cyclopentanecarboxylic acid ethyl ester (3.00 g, 19.2 mmol) in ethanol (20 mL) was treated with cyclopentylamine (1.90 mL, 19.2 mmol), sodium cyanoborohydride (2.42 g, 38.4 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) and 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-cyclopentylamino-cyclopentanecarboxylic acid ethyl ester (1.48 g, 6.57 mmol, 34.2%), as a light yellow oil. LC-MS (ESI) calcd for C13H23NO2 225.17, found 226.2 [M+H+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582626B2
Source datasetuspto-grants-2009_09
ORD IDord-554d50edfb7b4fe796c28807b1e2c38d
Source noteuspto-grants-2009_09