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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1601375Generated: October 30, 2026

p-(Trifluoromethoxy)benzaldehyde → 4-(TRIFLUOROMETHOXY)CINNAMIC ALDEHYDE

https://huagongshe.com/reaction/1601375

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-(Trifluoromethoxy)benzaldehydeHCID 69573—
Reactant(Triphenylphosphoranylidene)acetaldehydeHCID 75051—
SolventTolueneHCID 1140—
Product4-(TRIFLUOROMETHOXY)CINNAMIC ALDEHYDEHCID 1075119160%

Reaction Steps

570 mg (3.0 mmol) of 4-(trifluoromethoxy)benzaldehyde and 913 mg (3.0 mmol) of (triphenylphosphoranylidene)acetaldehyde were heated under reflux in 7.5 ml of toluene under nitrogen atmosphere for 1 hour and 45 minutes. The toluene was distilled off under reduced pressure and the thus obtained residue was purified over column chromatography using 20 g of silica gel. The fractions eluted with a mixed solvent of acetic acid-hexane (1:10) were collected to obtain 387 mg (yield: 60%) of the title compound as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05977152
Source datasetuspto-grants-1999_11
ORD IDord-9f7c1ed42f88469084c4596d1c1e314d
Source noteuspto-grants-1999_11