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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1662497Generated: October 29, 2026

Triethyl phosphonoacetate → (E)-Ethyl 3-cyclobutylacrylate

https://huagongshe.com/reaction/1662497

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethyl phosphonoacetateHCID 13345—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantLithium ChlorideHCID 433294—
ReactantCyclobutanecarbaldehydeHCID 12431621—
SolventAcetonitrileHCID 6342—
Product(E)-Ethyl 3-cyclobutylacrylateHCID 5770649294%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030354B2
Source datasetuspto-grants-2011_10
ORD IDord-6a7b0f6c26ab4ee99e6382156fa2025b
Source noteuspto-grants-2011_10