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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 602023Generated: October 31, 2026

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

https://huagongshe.com/reaction/602023

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 numberUS07902400B2
Source datasetuspto-grants-2011_03
ORD IDord-11a02a62a95a423a950f9d749a3ad604
Source noteuspto-grants-2011_03