HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1662497Generated: October 29, 2026
Triethyl phosphonoacetate → (E)-Ethyl 3-cyclobutylacrylate
https://huagongshe.com/reaction/1662497
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethyl phosphonoacetate | HCID 13345 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | Cyclobutanecarbaldehyde | HCID 12431621 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | (E)-Ethyl 3-cyclobutylacrylate | HCID 57706492 | 94% |
Reaction Steps
To a suspension of lithium chloride (2.22 g, 52.2 mmol) in MeCN (80 mL) were added ethyl 2-(diethoxyphosphoryl)acetate (available from Aldrich) (8.37 mL, 41.8 mmol) and DBU (16.7 mL, 111 mmol) at room temperature. The mixture was cooled to 0° C., and to it was added cyclobutanecarbaldehyde 70.B (2.93 g, 34.8 mmol) dropwise. The resulting cloudy mixture was warmed to room temperature and stirred overnight. The mixture was partitioned between water and EtOAc. The layers were separated, and the aqueous phase was extracted with additional EtOAc. The combined organic layers were washed with water and brine, dried (MgSO4), and concentrated. The residue was purified by silica gel flash chromatography (0-10% EtOAc/hexane) to afford (E)-ethyl 3-cyclobutylacrylate 70.C as a colorless liquid (5.00 g, 94%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08030354B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-6a7b0f6c26ab4ee99e6382156fa2025b |
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| Source note | uspto-grants-2011_10 |
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