Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2193437Generated: October 25, 2026

Isopropanol → 1-Chloro-3-(4-fluorophenyl)hex-5-en-3-ol

https://huagongshe.com/reaction/2193437

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropanolHCID 3776—
ReactantBinolHCID 11762—
Reactant2-Chloro-4'-fluoropropiophenoneHCID 67672—
ReactantTetrallylstannaneHCID 81878—
CatalystTitanium isopropoxideHCID 11026—
SolventDichloromethaneHCID 6344—
Product1-Chloro-3-(4-fluorophenyl)hex-5-en-3-olHCID 53472938—

Reaction Steps

To a solution of 1,1′-bi-2-naphthol (0.2280 g, 0.80 mmol, 0.26 equiv), CH2Cl2 (5 mL) and titanium(IV) isopropoxide (0.2243 g, 0.79 mmol, 0.26 equiv) were added 2-propanol (3.1620 g, 52.6 mmol, 17 equiv), tetraallylstannane (1.2538 g, 4.43 mmol, 1.43 equiv), and 3-chloro-1-(4-fluorophenyl)propan-1-one (0.5760 g, 3.09 mmol, 1.0 equiv) successively. The reaction mixture was stirred at rt under nitrogen for 22 h. The reaction was quenched with satd aq NH4Cl and extracted with EtOAc. The organic layer was dried over Na2SO4. After the solvents were evaporated, the residue was purified by chromatography on silica gel eluted with hexanes/ethyl acetate to afford 1-chloro-3-(4-fluorophenyl)hex-5-en-3-ol as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08329897B2
Source datasetuspto-grants-2012_12
ORD IDord-0ebaf5c72b6e433c9539bca7e2ac4ed8
Source noteuspto-grants-2012_12