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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 731356Generated: October 25, 2026

Ethyl 2-oxocyclopentanecarboxylate → 2-(Cyclobutylmethyl-amino)-cyclopentanecarboxylic acid ethyl ester

https://huagongshe.com/reaction/731356

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-oxocyclopentanecarboxylateHCID 69136—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium AcetateHCID 517045—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant1-Cyclobutylmethanamine hydrochlorideHCID 21707944—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
Product2-(Cyclobutylmethyl-amino)-cyclopentanecarboxylic acid ethyl esterHCID 5767119379.3%

Reaction Conditions

Temperature25 °C

Reaction Steps

2-Oxo-cyclopentanecarboxylic acid ethyl ester (0.24 mL, 1.64 mmol) and C-cyclobutyl-methylamine hydrochloride (0.20 g, 1.64 mmol) were dissolved in methanol (8 mL). Sodium acetate (0.27 g, 3.28 mmol) was added followed by 4 Å powdered molecular sieves (0.20 g) and sodium cyanoborohydride (0.21 g, 3.28 mmol). The reaction was stirred at 25° C. for 16 h. The mixture was poured into a mixture of saturated aqueous sodium bicarbonate solution (20 mL) and ethyl acetate (30 mL). After shaking, both layers were passed through a plug of Celite. The organic layer was further washed with saturated aqueous sodium bicarbonate solution (10 mL), saturated aqueous brine solution (10 mL), dried over magnesium sulfate, filtered, and concentrated in vacuo to afford the crude product, 2-(cyclobutylmethyl-amino)-cyclopentanecarboxylic acid ethyl ester (0.29 g, 1.30 mmol, 79%) as a clear oil. LC-MS (ESI) calcd for C13H23NO2 225.33, found 226.2 [M+H+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582626B2
Source datasetuspto-grants-2009_09
ORD IDord-39d5dcb038e94f0c92c9043f90f7fa5c
Source noteuspto-grants-2009_09