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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 375928Generated: October 30, 2026

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

https://huagongshe.com/reaction/375928

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 numberUS05488061
Source datasetuspto-grants-1996_01
ORD IDord-785384729be3452b93f6867e4d24a25f
Source noteuspto-grants-1996_01