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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 253098Generated: October 30, 2026

Acetic Acid → Benzyl 1-cyclopentylpiperidine-3-carboxylate

https://huagongshe.com/reaction/253098

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantCyclopentanoneHCID 8452—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantBenzyl piperidine-3-carboxylateHCID 13419237—
Solvent1,2-DichloroethaneHCID 11—
ProductBenzyl 1-cyclopentylpiperidine-3-carboxylateHCID 66844606—

Reaction Steps

The crude amine from the above step was dissolved in 1,2-dichloroethane (15 mL) and cyclopentanone (1.0 mL) was added via syringe. The reaction was allowed to stir for 5 min before the addition of HOAc (0.6 mL) and NaBH(OAc)3 (2.3 g, 10.9 mmol) in one portion. The reaction was allowed to stir for 48 h and then quenched with Na2CO3 (10%, 20 mL) and the reaction was allowed to stir for 1 h before being extracted with DCM (3×50 mL). The combined organics were washed with brine (sat, 200 mL), dried with sodium sulfate, filtered, concentrated to provide 1.3 g of crude oil that was purified by a 120 g Isco normal phase column (100% EtOAc) to give benzyl 1-cyclopentylpiperidine-3-carboxylate as a colorless oil. MS m/z: 288 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07872009B2
Source datasetuspto-grants-2011_01
ORD IDord-3c93f273449f43acb84c08a258680b98
Source noteuspto-grants-2011_01