Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2088247Generated: November 1, 2026

Ammonia → 4'-(4-Butoxy-2,3-difluorophenyl)-bicyclohexanol

https://huagongshe.com/reaction/2088247

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantEthyl AcetateHCID 8857—
ReactantAluminium lithium hydrideHCID 21226445—
Reactant4'-(4-Butoxy-2,3-difluorophenyl)-bicyclohexyl-4-oneHCID 66683775—
SolventTetrahydrofuranHCID 8028—
Product4'-(4-Butoxy-2,3-difluorophenyl)-bicyclohexanolHCID 67434326—

Reaction Steps

Lithium aluminum hydride (0.62 g) was suspended in THF (200 ml). 4′-(4-Butoxy-2,3-difluorophenyl)-bicyclohexyl-4-one (s-7) (10.0 g) was added dropwise to the suspension in the temperature range of −20° C. to −10° C., and the stirring was continued in this temperature range for 2 hours. After the completion of the reaction had been confirmed by means of GC analysis, ethyl acetate and then a saturated aqueous solution of ammonia were added to the reaction mixture under ice-cooling and deposits were removed by filtration through Celite. The filtrate was extracted with ethyl acetate. The combined organic phase was washed successively with water and brine, and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure and the residue was purified by recrystallization from heptane to give 4′-(4-butoxy-2,3-difluorophenyl)-bicyclohexanol (s-22) (8.8 g). The yield based on the compound (s-7) was 87.5%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08435422B2
Source datasetuspto-grants-2013_05
ORD IDord-b609f6659a65442991c113ccc80c9af3
Source noteuspto-grants-2013_05