Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1510890Generated: October 27, 2026

Cyclohexane, (bromomethyl)- → 1-Cyclohexyl-4-(5-fluoro-2-methoxyphenyl)-4-methylpentan-2-one

https://huagongshe.com/reaction/1510890

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexane, (bromomethyl)-HCID 137636—
Reactant3-(5-Fluoro-2-methoxyphenyl)-3-methyl-1-morpholin-4-ylbutan-1-oneHCID 22398528—
ReactantHCID 178418306HCID 178418306—
SolventTetrahydrofuranHCID 8028—
Product1-Cyclohexyl-4-(5-fluoro-2-methoxyphenyl)-4-methylpentan-2-oneHCID 2239862658.4%

Reaction Conditions

Temperature-70 °C

Reaction Steps

To a solution of cyclohexylmethyl bromide (0.26 g) in THF (1 mL) cooled to −70° C. under argon, tert-butyl lithium (1.7 M in pentane, 1.8 mL) was added dropwise over 5 minutes. The mixture was stirred at −70° C. for 30 minutes. A solution of 3-(5-fluoro-2-methoxyphenyl)-3-methyl-1-morpholin-4-ylbutan-1-one (0.33 g) in THF (1 mL) was added all at once and the mixture was stirred for one hour. The reaction temperature rose to approximately coming to −20° C. The reaction was quenched with EtOH (0.3 mL), and warmed to room temperature. The mixture was diluted with EtOAc, washed with water, dried, filtered, and evaporated. Chromatography of the residue over silica gel (eluent: hexanes-methylene chloride gradient) gave the title compound as an oil (0.2 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08212040B2
Source datasetuspto-grants-2012_07
ORD IDord-4913e1531de34d69a5e4b54a54685d7b
Source noteuspto-grants-2012_07