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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 650658Generated: October 28, 2026

4-Methylmorpholine → tert-Butyl 4-[(2E)-4-methoxy-4-oxobut-2-en-1-yl]piperidine-1-carboxylate

https://huagongshe.com/reaction/650658

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantAcetic acid, 2-(triphenylphosphoranylidene)-, methyl esterHCID 17453—
ReactantOxalyl chlorideHCID 65578—
Reactant1-(tert-Butoxycarbonyl)-4-(2-hydroxyethyl)piperidineHCID 854140—
SolventDimethyl SulfoxideHCID 679—
SolventDichloromethaneHCID 6344—
Producttert-Butyl 4-[(2E)-4-methoxy-4-oxobut-2-en-1-yl]piperidine-1-carboxylateHCID 10446560—

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of oxalyl chloride (11.8 g) in methylene chloride (180 ml) is cooled to −78° C. and dimethyl sulfoxide (DMSO) (8.9 ml) is added dropwise. The solution is stirred at −78° C. for about 3 minutes and a solution of N-BOC-2-(piperidin-4-yl)ethanol (14.3 g) in methylene chloride (250 ml) is added over a period of about 10 minutes. The solution is stirred for about 1 hour and N-methyl morpholine (21.6 g) is added over a period of about 15 minutes. The solution is allowed to warm to room temperature and, after about 30 minutes, methyl (triphenylphosphoranylidene) acetate (68.6 g) is added. The solution is stirred at room temperature for about 18 hours, evaporated in vacuo and the residue taken up in ethyl acetate. The ethyl acetate solution is washed with water, 5% HCl, 5% sodium hypochlorite solution, water, brine, dried over sodium sulfate, filtered and evaporated in vacuo to give methyl 4-(N-BOC-piperidin-4-yl)trans-crotonate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06274705B1
Source datasetuspto-grants-2001_08
ORD IDord-5077ae63f0b24a1f893c35e0329750d0
Source noteuspto-grants-2001_08