Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1079071Generated: November 2, 2026

Tetrahydrofuran → trans-3-[3-(1-Dodecynyl)phenyl]propen-1-ol

https://huagongshe.com/reaction/1079071

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl trans-3-[3-(1-Dodecynyl)phenyl]-2-propenoateHCID 18373045—
ReactantDiisobutylaluminumhydrideHCID 21225700—
SolventEthyl AcetateHCID 8857—
Producttrans-3-[3-(1-Dodecynyl)phenyl]propen-1-olHCID 1837290781.5%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of ethyl trans-3-[3-(1-dodecynyl)phenyl]-2-propenoate (10.0 g) and dry tetrahydrofuran (100 ml) at -78° C. was added diisobutylaluminum hydride (1.5M in toluene) (49 ml) slowly. The reaction mixture was stirred for 20 mins at -78° C., and 25% sodium hydroxide solution (3 ml) was added. The mixture was slowly warmed to room temperature and an additional 25% sodium hydroxide solution (3 ml) was added. The mixture was diluted with ethyl acetate and washed with water and brine. The organic phase was separated, dried over anhydrous magnesium sulfate, filtered, and the filtrate was concentrated in vacuo. The residue was flash chromatographed over silica gel (eluted with ethyl acetate/hexane/1:3). The appropriate fractions were collected and evaporated to afford 7.14 g (81%) of product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05550247
Source datasetuspto-grants-1996_08
ORD IDord-3ff7827ccc724faf95aba26fb8e89d3b
Source noteuspto-grants-1996_08