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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1876938Generated: October 26, 2026

{2-Ethyl-5-[4-(trifluoromethyl)phenyl]-3-furyl}methanol → 2-Ethyl-5-[4-(trifluoromethyl)phenyl]-3-furaldehyde

https://huagongshe.com/reaction/1876938

Reaction equation

Participants

RoleNameHCIDCharge
Reactant{2-Ethyl-5-[4-(trifluoromethyl)phenyl]-3-furyl}methanolHCID 23074480—
CatalystHCID 178418406HCID 178418406—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product2-Ethyl-5-[4-(trifluoromethyl)phenyl]-3-furaldehydeHCID 2307435524.6%

Reaction Conditions

Temperature40 °C

Reaction Steps

A suspension of {2-ethyl-5-[4-(trifluoromethyl)phenyl]-3-furyl}methanol (2.7 g) and manganese dioxide (6.8 g) in diethyl ether (20 mL) and tetrahydrofuran (20 mL) was stirred overnight at 40° C. Manganese dioxide was filtered off, and the filtrate was evaporated under reduced pressure. The residue was purified by silica gel chromatography (5% ethyl acetate/hexane to 20% ethyl acetate/hexane), and crystallized from ethyl acetate/hexane to give the title compound (0.66 g, 24%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08309580B2
Source datasetuspto-grants-2012_11
ORD IDord-702d166f9b8142d3b86b750a9e79e101
Source noteuspto-grants-2012_11