Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1095242Generated: November 2, 2026

Hydrochloric Acid → HCID 18787929, compound

https://huagongshe.com/reaction/1095242

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl AcetateHCID 8857—
ReactantBenzenesulfinic acid, sodium saltHCID 2723840—
ReactantMagnesiumHCID 5462224—
Reactant4'-(2-Fluoro-4-(4-pentylcyclohexyl)phenyl)bi(cyclohexane)-4-olHCID 66781460—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18787929HCID 18787929—

Reaction Conditions

Temperature50 °C

Reaction Steps

Well-dried magnesium (8.3 g) and THF (20 ml) were put in a reaction vessel under a nitrogen atmosphere, and heated to 50° C. 1-Bromo-3-fluorobenzene (14) (60.0 g) dissolved in THF (300 ml) was slowly added dropwise thereto in the temperature range of 40° C. to 60° C., and the mixture was stirred for another 60 minutes. Then, 1,4-dioxaspiro[4.5]decan-8-one (15) (64.3 g) dissolved in THF (150 ml) was slowly added dropwise thereto in the temperature range of 50° C. to 60° C., and the mixture was stirred for another 60 minutes. The reaction mixture was cooled to 30° C., and then poured into a vessel containing an aqueous 1N—HCl solution (900 ml) and ethyl acetate (500 ml), and mixed. The mixture was then allowed to stand until it had separated into two phases, the organic and aqueous phases, and an extractive operation to an organic phase was carried out. The organic phase was fractionated, and washed sequentially with water and a saturated aqueous solution of sodium hydrogencarbonate and water, and then dried over anhydrous magnesium sulfate. The solvent was then distilled off under reduced pressure, giving 74.6 g of 8-(3-fluorophenyl)-1,4-dioxaspiro[4,5]decan-8-ol (16).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08137583B2
Source datasetuspto-grants-2012_03
ORD IDord-498e141ccc1b4b84949546e0c697428a
Source noteuspto-grants-2012_03