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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 977552Generated: October 29, 2026

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

https://huagongshe.com/reaction/977552

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 wits 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 numberUS05614631
Source datasetuspto-grants-1997_03
ORD IDord-f6e6fa857f2b41719579b7ce08dd9b40
Source noteuspto-grants-1997_03