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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic acid, 2-(triphenylphosphoranylidene)-, ethyl ester | HCID 70670 | — |
| Reactant | tert-Butyl 4-oxopiperidine-1-carboxylate | HCID 735900 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | tert-Butyl 4-(2-ethoxy-2-oxoethylidene)piperidine-1-carboxylate | HCID 10333298 | 88.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06555570B2 |
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| Source dataset | uspto-grants-2003_04 |
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| ORD ID | ord-a583002ca37a44dcaf61026665cd1a5a |
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| Source note | uspto-grants-2003_04 |
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