Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1601357Generated: October 31, 2026

ethyl (4E)-3-methyl-5-[4-(trifluoromethyl)phenyl]-2,4-pentadienoate → (2E,4E)-3-Methyl-5-[4-(trifluoromethyl)phenyl]-2,4-pentadien-1-ol

https://huagongshe.com/reaction/1601357

Reaction equation

Participants

RoleNameHCIDCharge
Reactantethyl (4E)-3-methyl-5-[4-(trifluoromethyl)phenyl]-2,4-pentadienoateHCID 86583786—
ReactantDiisobutylaluminumhydride tolueneHCID 86583787—
SolventTolueneHCID 1140—
Product(2E,4E)-3-Methyl-5-[4-(trifluoromethyl)phenyl]-2,4-pentadien-1-olHCID 5997056070.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

After a solution in which 150 mg (0.53 mmol) of ethyl (4E)-3-methyl-5-[4-(trifluoromethyl)phenyl]-2,4-pentadienoate ((2E)/(2Z)=5/1) as described in Reference example 8 were dissolved in 2 ml of toluene was stirred at 0° C., 0.7 ml (1.06 mmol) of a 1.5M diisobutyl aluminum hydride-toluene solution were added to the solution. After 20 minutes, ice-water was added to the reaction mixture and the mixture was stirred for 10 minutes. The insolubles were removed by filtration using Celite and the filtrate was extracted with ethyl acetate and dried, followed by evaporation of the solvent to obtain an oil. The oil was subjected to column chromatography using 5 g of silica gel and eluted with a mixed solvent of 30 to 40% ethyl acetate-hexane to obtain 90 mg of the title compound as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05977152
Source datasetuspto-grants-1999_11
ORD IDord-122227432ab94931b5296799bff98018
Source noteuspto-grants-1999_11