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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 366183Generated: October 30, 2026

Acetic acid, 2-(triphenylphosphoranylidene)-, ethyl ester → tert-Butyl 4-(2-ethoxy-2-oxoethylidene)piperidine-1-carboxylate

https://huagongshe.com/reaction/366183

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic acid, 2-(triphenylphosphoranylidene)-, ethyl esterHCID 70670—
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
SolventTolueneHCID 1140—
Producttert-Butyl 4-(2-ethoxy-2-oxoethylidene)piperidine-1-carboxylateHCID 1033329888.8%

Reaction Steps

4-Oxopiperidine-1-carboxylic acid tert-butyl ester (8.0 g; 40.2 mmol) was dissolved in toluene (80 mL). Carboethoxymethylene triphenylphosphorane (17.5 g; 50.2 mmol) was added and the reaction mixture was heated 12 hours at reflux. The reaction mixture was evaporated in vacuo and the residue was chromatographed on silica (4.5×30 cm) using diethyl ether/heptane (1:1) as eluent to afford 9.5 g (35.7 mmol) of 4-Ethoxycarbonylmethylenepiperidine-1-carboxylic acid tert-butyl ester, which was dissolved in 1,4-dioxane and cooled to 0° C. Lithium hydroxide (2.73 g; 114 mmol) was dissolved in water (20 mL) and added. The reaction mixture was stirred for 12 hours at room temperature. Ethyl acetate (200 mL) and water (100 mL) was added. Sodium hydrogen sulfate (10%; aqueous solution) was added to pH 2. The organic phase was washed with water (100 mL), dried (magnesium sulfate) and evaporated in vacuo to afford 5.49 g of 4-carboxymethylenepiperidine-1-carboxylic acid tert-butyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06127391
Source datasetuspto-grants-2000_10
ORD IDord-d4c837b73578463eadfa562589d07363
Source noteuspto-grants-2000_10