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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 381447Generated: October 31, 2026

(E)-5-[4-(Trifluoromethyl)phenyl]-2-penten-4-yn-1-ol → (E)-5-(4-(Trifluoromethyl)phenyl]-2-penten-4-ynal

https://huagongshe.com/reaction/381447

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(E)-5-[4-(Trifluoromethyl)phenyl]-2-penten-4-yn-1-olHCID 18363296—
CatalystHCID 178418406HCID 178418406—
SolventDichloromethaneHCID 6344—
Product(E)-5-(4-(Trifluoromethyl)phenyl]-2-penten-4-ynalHCID 1836329370.1%

Reaction Steps

In 4 ml of methylene chloride were dissolved 350 mg (1.56 mmol) of (E)-5-[4-(trifluoromethyl)phenyl]-2-penten-4-yn-1-ol, and 3.5 g of active manganese dioxide were added to the solution, followed by stirring of the resulting mixture at room temperature for 30 minutes. The solid was removed by filtration and the filtrate was concentrated. Then, the filtrate was subjected to column chromatography using 10 g of silica gel and eluted with a mixed solvent of ethyl acetate-hexane (1:214) to obtain 245 mg (yield: 70%) of the title compound as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06306880B1
Source datasetuspto-grants-2001_10
ORD IDord-b49d2c27b031433cbee52bc4c5b41292
Source noteuspto-grants-2001_10