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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 223768Generated: October 25, 2026

Potassium Carbonate → HCID 54353582, compound

https://huagongshe.com/reaction/223768

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 3-formylbenzoateHCID 639145—
ReactantPhosphonium, [[3-(methoxycarbonyl)phenyl]methyl]triphenyl-, bromideHCID 10051285—
CatalystTetrabutylammonium IodideHCID 67553—
SolventDichloromethaneHCID 6344—
ProductHCID 54353582HCID 5435358282.3%

Reaction Steps

To a mixture of 49.2 g (0.3 mole) of m-carbomethoxybenzaldehyde, 221 g (0.45 mole) of m-carbomethoxybenzyl triphenyl phosphonium bromide and 1.0 g of tetrabutyl ammonium iodide in 500 ml of dichloromethane, 500 ml of 50% solution of potassium carbonate was added. The mixture was stirred at room temperature for 3 hr. The alkaline layer was separated, extracted with dichloromethane and the combined organic solvent was washed with plenty of water and dried. Evaporation of the solvent and recrystallization of the residue from ether gave 73.2 g of white needles of predominantly transisomer. Yield 82%. m.p. softens at 64° C. and melts at 105°-107° C. The infrared spectrum showed absorption at 1720 cm-1 (COOCH3), 1675 cm-1 (trans c=c), 965 cm-1 (trans c=c) and 670 cm-1 (weak cis c=c). NMR (CDCl3) showed 3.9-4.0 (d. COOCH3, 6) 67-72 (d, CH=CH, 2) and 7.3-8.4 (m, aromatic, 8). Anal. calcd. for C18H16O4 : C, 72.97%, H, 5.40. Found: C, 73.02%, H, 5.41%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04356292
Source datasetuspto-grants-1982_10
ORD IDord-422948f4f0454b159875da2801ece371
Source noteuspto-grants-1982_10