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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1268554Generated: October 30, 2026

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

https://huagongshe.com/reaction/1268554

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 4carboxymethylenepiperidine-1-carboxylic acid tert-butyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06555570B2
Source datasetuspto-grants-2003_04
ORD IDord-a583002ca37a44dcaf61026665cd1a5a
Source noteuspto-grants-2003_04