Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 641105Generated: October 30, 2026

Hydrochloric Acid → 1-(3-Chloro-4-ethoxy-2-fluorophenyl)-4-vinylcyclohexanol

https://huagongshe.com/reaction/641105

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4-EthenylcyclohexanoneHCID 543953—
ReactantMagnesiumHCID 5462224—
Reactant1-Bromo-3-chloro-4-ethoxy-2-fluorobenzeneHCID 53414984—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
Product1-(3-Chloro-4-ethoxy-2-fluorophenyl)-4-vinylcyclohexanolHCID 59256973133%

Reaction Conditions

Temperature40 °C

Reaction Steps

1.5 g of well dried magnesium and 30 mL of THF were placed in a reactor under nitrogen atmosphere, and heated to 40° C. 15.3 g of the compound (1) dissolved in 30 mL of THF was slowly added dropwise thereto at a temperature range of from 35 to 49° C., followed by stirring for 30 minutes. Thereafter, 5.0 g of the compound (23) dissolved in 5 mL of THF was slowly added dropwise thereto at a temperature range of from 30 to 40° C., followed by stirring for 30 minutes. After cooling the resulting reaction mixture to 25° C., the reaction mixture was poured into and mixed with a mixture of 100 mL of 1N hydrochloric acid and 100 mL of toluene. The mixture was separated into an organic layer and an aqueous layer by standing still, so as to attain extraction to the organic layer. The resulting organic layer was fractionated and washed with water, a 2N sodium hydroxide aqueous solution, a saturated sodium bicarbonate aqueous solution and water, followed by drying over anhydrous magnesium sulfate. Thereafter, the solvent was removed by distillation under reduced pressure to obtain 16.0 g of 1-(3-chloro-4-ethoxy-2-fluorophenyl)-4-vinylcyclohexanol (24) as a yellow liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07695777B2
Source datasetuspto-grants-2010_04
ORD IDord-bf38e898c8134e688e842add4bf3be3d
Source noteuspto-grants-2010_04