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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1383234Generated: November 3, 2026

3-Phenoxybenzaldehyde → HCID 54170266, compound

https://huagongshe.com/reaction/1383234

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-PhenoxybenzaldehydeHCID 38284—
ReactantAcetic acid, 2-(triphenylphosphoranylidene)-, ethyl esterHCID 70670—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
SolventEthylacetate heptaneHCID 21899848—
ProductHCID 54170266HCID 5417026676.5%

Reaction Steps

To a stirred solution of 23.4 g (0.188 mole) of 3-phenoxybenzaldehyde in 175 mL of 1,4-dioxane was added 45.2 grams (0.130 mole) of ethoxycarbonylmethylenetriphenylphosphorane in one portion. The reaction was allowed to stir at ambient temperature overnight. The solvent was evaporated under reduced pressure, leaving a residue which was dissolved in ethyl acetate. Approximately 30 grams of silica gel was mixed with this solution. This solvent was evaporated under reduced pressure, and the silica gel was placed in a sintered glass filter. The silica gel was eluted with 1000 mL of heptane/ethyl acetate (3:1). The solvent was evaporated under reduced pressure, leaving an oil. This oil was dissolved in 150 mL of heptane/ethyl acetate (9:1), treated with 15 grams of silica gel, and filtered. The filtrate was evaporated under reduced pressure, leaving 26.7 grams of ethyl 3-(3-phenoxyphenyl)acrylate as an oil. The nmr spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04808762
Source datasetuspto-grants-1989_02
ORD IDord-d2b3a63024c34541a63ef7124881eb0f
Source noteuspto-grants-1989_02