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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 379956Generated: October 30, 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/379956

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 (1:24) to obtain 245 mg (yield: 70%) of the title compound as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06300357B1
Source datasetuspto-grants-2001_10
ORD IDord-9920da54fb77480c9c10d9e1b93d7a8c
Source noteuspto-grants-2001_10