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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 931302Generated: October 26, 2026

Triethylamine → cis-1-Tert-butyl 3-ethyl 4-methylpiperidine-1,3-dicarboxylate

https://huagongshe.com/reaction/931302

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantDi-tert-butyl dicarbonateHCID 90495—
ReactantEthyl 4-methylpiperidine-3-carboxylateHCID 13658603—
Reactant1-Tert-butyl 3-ethyl 4-methylpiperidine-1,3-dicarboxylateHCID 70791601—
SolventDichloromethaneHCID 6344—
Productcis-1-Tert-butyl 3-ethyl 4-methylpiperidine-1,3-dicarboxylateHCID 13173516483.3%

Reaction Steps

Di-tert-butyl dicarbonate (3.26 g, 15.20 mmol) was added to a solution of ethyl 4-methylpiperidine-3-carboxylate (2.0 g, 11.68 mmol) and triethylamine (3.9 mL, 28.05 mmol) in anhydrous dichloromethane (50 mL) at 0° C. The reaction mixture was stirred at room temperature for 18 h. The mixture partitioned between dichloromethane and water. The organics were dried over sodium sulfate, filtered and concentrated under reduced pressure to afford a mixture of the cis and trans diastereomers of 1-tert-butyl 3-ethyl 4-methylpiperidine-1,3-dicarboxylate (3.0 g). The crude material was purified via column chromatography (5-10% ethyl acetate in petroleum ether) to afford cis-1-tert-butyl 3-ethyl 4-methylpiperidine-1,3-dicarboxylate (2.5 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09296745B2
Source datasetuspto-grants-2016_03
ORD IDord-4a634299e5f74e8d8bc683344d04df11
Source noteuspto-grants-2016_03