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HRID 450960作成日:2026年10月24日

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

https://huagongshe.com/ja/reaction/450960

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/ethyl acetate 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US08487094B2
出典データセットuspto-grants-2013_07
ORD IDord-f38ad47adc164f30938f3185cfebd733
出典メモuspto-grants-2013_07