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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1282016Generated: October 28, 2026

Diethyl Ether → 1-t-Butoxycarbonyl-4-(2-cyclopentyl-2-hydroxyethyl)piperidine

https://huagongshe.com/reaction/1282016

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantCyclopentanoneHCID 8452—
ReactantAmmonium ChlorideHCID 25517—
ReactantTert-butyl 4-(iodomethyl)piperidine-1-carboxylateHCID 10448961—
ReactantHCID 178418306HCID 178418306—
Product1-t-Butoxycarbonyl-4-(2-cyclopentyl-2-hydroxyethyl)piperidineHCID 18423503—

Reaction Steps

To a solution of 1.36 g (4.2 mmol) of 1-t-butoxycarbonyl-4-iodomethylpiperidine in 40 mL of ether at −78° C. was carefully added 5.8 mL (9.35 mmol) of t-butyl lithium (1.7 N on pentane). After stirring for 30 min, to the reaction mixture was added dropwise 0.95 mL (10.73 mmol) of cyclopentanone and the reaction mixture was stirred at −78° C. for 2 h. To the reaction mixture was added 5 mL of sat'd NH4Cl solution and the reaction mixture was warmed to rt. The reaction mixture was partitioned between sat'd NH4Cl solution and ether. The aqueous fraction was extracted with ether and the combined organic fractions were washed with sat'd NaCl solution, dried over MgSO4, filtered and the filtrate was concentrated. The residue was purified by chromatography (silica, hexanes:ether, 4:1) to give 0.36 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06455548B2
Source datasetuspto-grants-2002_09
ORD IDord-f799b7bf98ca4e61a1c807b9fe88282d
Source noteuspto-grants-2002_09