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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2236375Generated: October 30, 2026

Acetonitrile → 3,5-Difluoro-4-(2-propynyloxy)benzaldehyde

https://huagongshe.com/reaction/2236375

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantPropargyl alcoholHCID 7859—
ReactantPotassium CarbonateHCID 11430—
Reactant3,4,5-TrifluorobenzaldehydeHCID 2776954—
SolventWaterHCID 962—
Product3,5-Difluoro-4-(2-propynyloxy)benzaldehydeHCID 57445667102%

Reaction Steps

To 50 ml of acetonitrile were added 12 g of propargyl alcohol, 16 g of 3,4,5-trifluorobenzaldehyde and 15 g of potassium carbonate, and the mixture obtained was stirred at room temperature for 1 day. Then, water was added to the reaction mixture and the mixture was extracted with ethyl acetate. The organic layer was washed with dilute hydrochloric acid and brine. The organic layer was dried over magnesium sulfate and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to obtain 20 g of 3,5-difluoro-4-(2-propynyloxy)benzaldehyde represented by the formula:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07714168B2
Source datasetuspto-grants-2010_05
ORD IDord-f6b365fa758a4b6282d372d4eb8767e1
Source noteuspto-grants-2010_05