HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1248722Generated: October 30, 2026
Acetic Acid → Ethyl 2-(2-methoxycarbonylbenzyliden)-4,4-diethoxyacetoacetate
https://huagongshe.com/reaction/1248722
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Methyl 2-formylbenzoate | HCID 243003 | — |
| Reactant | Ethyl 4,4-diethoxy-3-oxobutanoate | HCID 11138577 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | Ethyl 2-(2-methoxycarbonylbenzyliden)-4,4-diethoxyacetoacetate | HCID 54462958 | 116.3% |
Reaction Steps
To a mixture of methyl 2-formylbenzoate (4.92 g), ethyl 4,4-diethoxyacetoacetate (7.2 g) and acetic acid (0.36 g) in benzene (15 ml) was added portionwise each one third portion of a solution of piperidine (306 mg) in benzene (5 ml) for each 20 minutes' interval, and the mixture was heated to reflux for 3 hours under removing off azeotropically the resulting water. After cooling, the reaction mixture was diluted with additional benzene (25 ml), washed three times with water and successively with diluted aqueous sodium bicarbonate solution, water and saturated aqueous sodium chloride solution and dried over magnesium sulfate. The solvent was distilled off under reduced pressure to give reddish oil (12.7 g) of crude ethyl 2-(2-methoxycarbonylbenzyliden)-4,4-diethoxyacetoacetate which was used in the following reaction without any further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04525478 |
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| Source dataset | uspto-grants-1985_06 |
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| ORD ID | ord-5be5a6fb8c7a42ee840b3335f53b6437 |
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| Source note | uspto-grants-1985_06 |
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