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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1795168Generated: November 2, 2026

Trimethyl phosphonoacetate → 4-Cyclohexyl-4-(2-methoxycarbonyl-vinyl)-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1795168

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethyl phosphonoacetateHCID 80029—
ReactantLithium ChlorideHCID 433294—
Reactant1,8-Diazabicyclo[4.3.0]non-7-eneHCID 15788991—
Reactant4-Cyclohexyl-4-formylpiperidine-1-carboxylic acid tert-butyl esterHCID 21936875—
SolventAcetonitrileHCID 6342—
Product4-Cyclohexyl-4-(2-methoxycarbonyl-vinyl)-piperidine-1-carboxylic acid tert-butyl esterHCID 6959711086%

Reaction Steps

To a solution of trimethyl phosphonoacetate (1.41 ml, 8.72 mmole), lithium chloride (477 mg, 11.3 mmole), and 1,8-diazabicyclo[4.3.0]non-7-ene (DBU) (1.55 ml, 11.3 mmole) in anhydrous acetonitrile (25 ml) is added 4-cyclohexyl-4-formyl-piperidine-1-carboxylic acid tert-butyl ester, 7, (2.58 mg, 8.72 mmole) under argon at room temperature. The mixture is stirred for one hour and the solvent then removed under reduced pressure. The crude product is purified over silica (methylene chloride:methanol=15:1, Rf=0.78) to afford 2.64 g (86% yield) of the desired compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07026335B2
Source datasetuspto-grants-2006_04
ORD IDord-94b6c078e4e946cab61a484cb6848c8b
Source noteuspto-grants-2006_04