Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1601385Generated: October 30, 2026

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

https://huagongshe.com/reaction/1601385

Reaction equation

Participants

RoleNameHCIDCharge
Reactantethyl (E)-5-[4-(trifluoromethyl)phenyl]-2-penten-4-ynoateHCID 20693054—
ReactantDiisobutylaluminumhydride tolueneHCID 86583787—
SolventTolueneHCID 1140—
Product(E)-5-[4-(Trifluoromethyl)phenyl]-2-penten-4-yn-1-olHCID 1836329687.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

In 4 ml of toluene were dissolved 480 mg (1.79 mmol) of ethyl (E)-5-[4-(trifluoromethyl)phenyl]-2-penten-4-ynoate, and 2.38 ml (3.58 mmol) of a 1.5M diisobutyl aluminum hydride-toluene solution were added to the solution with stirring at 0° C. After 10 minutes, ice was added to the mixture and the insolubles were removed by filtration using Celite. After the organic layer was dried, the crude product obtained by evaporation of the solvent was subjected to column chromatography using 15 g of silica gel and eluted with a mixed solvent of ethyl acetate-hexane (3:17) to obtain 353 mg (yield: 87%) of the title compound as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05977152
Source datasetuspto-grants-1999_11
ORD IDord-fbbe37fe9bce4b42a1b11dde3634db17
Source noteuspto-grants-1999_11