HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2178752Generated: October 29, 2026
Ethanol → ethyl 2-acetyl-3-ethoxybut-2-enoate
https://huagongshe.com/reaction/2178752
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Ethyl Acetoacetate | HCID 8868 | — |
| Reactant | 1,1-Diethoxyethene | HCID 137673 | — |
| Catalyst | Sodium ethoxide | HCID 2723922 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | ethyl 2-acetyl-3-ethoxybut-2-enoate | HCID 231474 | 89% |
Reaction Steps
A 5 L 4-neck flask equipped with a mechanical stirrer, condenser, thermowell, addition funnel and N2 inlet was charged with ethyl acetoacetate (493.1 g, 483 mL, 3.7931 mol, 1.0 equiv) and sodium ethoxide (3.1 g, 0.046 mol, 1.2 mol %). Ketene diethylacetal (880.0 g, 1000 mL, 7.5862 mol, 2.0 equiv) was added over 1 hr maintaining the reaction temperature at <22° C. by external cooling. When addition was complete, the reaction mixture was heated at 85° C.±5° C. for 7.5 hr. The yellow brown reaction mixture was cooled to room temperature and stirred overnight. Much of the lower boiling components [EtOH, EtOAc, Me(OEt)3] were stripped on a roto-evaporator (bath temperature ˜65° C.). The residual yellow-orange oil was distilled, collecting the fraction with bp 100-107° C. (1.8-2.1 Torr) to give 675.2 g (89%) of product as a yellow liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09067921B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-5f5f82ec29a9484ebf51e25907de1c90 |
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| Source note | uspto-grants-2015_06 |
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