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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 479209Generated: October 26, 2026

Potassium Carbonate → (Z)-3-(4-benzyloxy-2-methyl-phenyl)-2-ethoxy-acrylic acid ethyl ester

https://huagongshe.com/reaction/479209

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Methyl 4-benzyloxybenzaldehydeHCID 2759806—
ReactantPhosphonium, (1,2-diethoxy-2-oxoethyl)triphenyl-, chloride (1:1)HCID 11327835—
SolventIsopropanolHCID 3776—
Product(Z)-3-(4-benzyloxy-2-methyl-phenyl)-2-ethoxy-acrylic acid ethyl esterHCID 6861701860%

Reaction Conditions

Temperature60 °C

Reaction Steps

(Ethoxy-ethoxycarbonyl-methyl)-triphenyl-phosphonium chloride (3.79 g, 8.8 mmol) and potassium carbonate (1.46 g, 10.6 mmol) were added to a solution of 4-benzyloxy-2-methyl-benzaldehyde (0.8 g, 3.5 mmol) in isopropanol (10 ml) at 10° C. under an argon atmosphere [for the preparation of (ethoxy-ethoxycarbonyl-methyl)-triphenyl-phosphonium chloride see: K. K. Bach, H. R. El-Seedi, H. M. Jensen, H. B. Nielsen, I. Thomson, K. B. G. Torssell, Tetrahedron 1994, 50, 7543-7556]. The suspension was heated to 60° C. After 12 h and after 20 h (ethoxy-ethoxycarbonyl-methyl)-triphenyl-phosphonium chloride (each time 3.79 g, 8.8 mmol) and potassium carbonate (each time 1.46 g, 10.6 mmol) were added again. After 36 h the suspension was filtered off and the filtrate was evaporated under reduced pressure. The residue was dissolved in dichloromethane, washed with saturated aqueous ammonium chloride and ice water and dried over sodium sulfate. The solvent was removed under reduced pressure and the residue purified by column chromatography (silica gel, dichloromethane) to give 0.7 g (2.1 mmol, 58%) of the title compound as yellow liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06642389B2
Source datasetuspto-grants-2003_11
ORD IDord-97199bd2b93641ba9ba3bddf38e9bdee
Source noteuspto-grants-2003_11