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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1681130Generated: November 4, 2026

4-Methylbenzaldehyde → HCID 53981355, compound

https://huagongshe.com/reaction/1681130

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylbenzaldehydeHCID 7725—
ReactantAcetic AnhydrideHCID 7918—
Reactant1,1,1-Trichloro-2,2,2-trifluoroethaneHCID 9635—
CatalystZincHCID 23994—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 53981355HCID 53981355390.7%

Reaction Steps

12 g of p-tolualdehyde dissolved in 20 cc of DMF and 7.5 g of Zn are charged to a flask of 250 ml of capacity. 2.5 g of CF3CCl3 is dropwise added and the resulting reaction mixture is slightly heated until the reaction turns into strongly exothermic. Then 10 g of CF3CCl3 dissolved in 100 cc of DMF is dropwise added and the resulting mixture is stirred at room temperature for 4 hours. 10 cc of acetic anhydride and 13 g of Zn are then added. After 2 hours at room temperature, the reaction mixture is poured in acidic water and is extracted three times with ether; the ether phases are combined with one another, and are washed with a saturated solution of sodium bicarbonate, and with brine, and are then thoroughly dried and evaporated. The raw reaction product is chromatographed on silica (98/2 hexane/ethyl acetate). 11.5 g of 4-(2-chloro-3,3,3-trifluoroprop-1-enyl)-toluene is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05169848
Source datasetuspto-grants-1992_12
ORD IDord-a978f59029d24c7a8703d54b15d284c6
Source noteuspto-grants-1992_12