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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1484511Generated: October 31, 2026

4-Hydroxy-2-(trifluoromethoxy)benzaldehyde → HCID 68322507, compound

https://huagongshe.com/reaction/1484511

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Hydroxy-2-(trifluoromethoxy)benzaldehydeHCID 24721507—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventAcetic acid ethanolHCID 18476134—
ProductHCID 68322507HCID 68322507—

Reaction Steps

A solution of 4-hydroxy-2-(trifluoromethoxy)benzaldehyde (210 g, 1 equiv) in ethanol: acetic acid 3:1 (1050 Lt) was treated with Pd/C 5% catalyst-50% wet (21 g) and stirred at 800 rpm under 5 bar of hydrogen for 2.5 hrs. A second aliquot of Pd/C 5% catalyst-50% wet (33.6 g) was then added and the mixture subjected to the same hydrogenation conditions until reaching 22 hrs in total. The reaction mixture was filtered on a charcoal cartridge and washed with ethanol (525 mL). The resulting clear solution was concentrated to ca. 420 mL and the residue diluted with ethyl acetate (1050 Lt) and an aqueous 10% solution of ammonium chloride (525 mL). The phases were allowed separating and the organic one washed with water (2×525 mL), dried over sodium sulfate, filtered and concentrated to dryness. The title compound was obtained as colorless oil (196 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09422252B2
Source datasetuspto-grants-2016_08
ORD IDord-2930e7a3260548b1b2e2bedb8ccebebd
Source noteuspto-grants-2016_08