Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2093648Generated: November 1, 2026

4-Hydroxy-3-(trifluoromethoxy)benzaldehyde → HCID 58182218, compound

https://huagongshe.com/reaction/2093648

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Hydroxy-3-(trifluoromethoxy)benzaldehydeHCID 7018050—
ReactantJones' reagentHCID 131709961—
SolventAcetoneHCID 180—
ProductHCID 58182218HCID 58182218—

Reaction Steps

To a 0° C. solution of 4-hydroxy-3-(trifluoromethoxy)benzaldehyde (901 mg, 4.37 mmol) in acetone (10 ml) was added 4 ml of the Jones reagent. The ice bath was removed and the reaction was stirred at room temperature for ca. 1 h. Isopropanol was added to destroy the excess Jones reagent. The mixture was diluted with ethyl acetate, the precipitate was filtered off, and the filtrate concentrated in vacuo. The residue was diluted with 1M HCl and extracted 3 times with ethyl acetate. The combined organics were washed with brine, dried over sodium sulfate, and concentrated in vacuo to afford the title compound. Mass spectrum (ESI) 221.1 (M−1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08445480B2
Source datasetuspto-grants-2013_05
ORD IDord-61822ff9297246158a9e0b403bcda9ff
Source noteuspto-grants-2013_05