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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2037429Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/2037429

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIsopropanolHCID 3776—
EduktBinolHCID 11762—
Edukt2-Chloro-4'-fluoropropiophenoneHCID 67672—
EduktTetrallylstannaneHCID 81878—
KatalysatorTitanium isopropoxideHCID 11026—
LösungsmittelDichloromethaneHCID 6344—
Produkt1-Chloro-3-(4-fluorophenyl)hex-5-en-3-olHCID 53472938—

Reaktionsschritte

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/EtOAc to afford 1-chloro-3-(4-fluorophenyl)hex-5-en-3-ol as an oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08575156B2
Quelldatensatzuspto-grants-2013_11
ORD IDord-68f53296634847b78f8625e71ce4641c
Quellennotizuspto-grants-2013_11