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HRID 2037429作成日:2026年10月27日

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

https://huagongshe.com/reaction/2037429

反応式

関与物質

役割名称HCID仕込み量
反応物IsopropanolHCID 3776—
反応物BinolHCID 11762—
反応物2-Chloro-4'-fluoropropiophenoneHCID 67672—
反応物TetrallylstannaneHCID 81878—
触媒Titanium isopropoxideHCID 11026—
溶媒DichloromethaneHCID 6344—
生成物1-Chloro-3-(4-fluorophenyl)hex-5-en-3-olHCID 53472938—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08575156B2
出典データセットuspto-grants-2013_11
ORD IDord-68f53296634847b78f8625e71ce4641c
出典メモuspto-grants-2013_11