1-(4-Bromo-2-iodophenoxy)-5-chloropentan-2-one → 3-((4-Bromo-2-iodophenoxy)methyl)-6-chlorohex-1-en-3-ol
反応式
[Br:1][C:2]1[CH:15]=[CH:14][C:5]([O:6][CH2:7][C:8](=[O:13])[CH2:9][CH2:10][CH2:11][Cl:12])=[C:4]([I:16])[CH:3]=1.[CH:17]([Mg]Br)=[CH2:18]>C1COCC1>[Br:1][C:2]1[CH:15]=[CH:14][C:5]([O:6][CH2:7][C:8]([OH:13])([CH2:9][CH2:10][CH2:11][Cl:12])[CH:17]=[CH2:18])=[C:4]([I:16])[CH:3]=1参加物
4
反応条件
- 温度
- -78 °C
実験手順
To a solution of 1-(4-bromo-2-iodophenoxy)-5-chloropentan-2-one (1.61 g, 3.86 mmol) in THF (35 mL) was added vinylmagnesium bromide (1M solution in THF, 4.3 mL) at −78° C. under an argon atmosphere. After stirring for 1 hour at −78° C., the mixture was gradually warmed up to −30° C. over 1 hour. The reaction was quenched by adding saturated aqueous NH4Cl solution and extracted with EtOAc. The combined organic layer were washed with brine, dried over Na2SO4, filtered, and the filtrate was evaporated. The residue was purified by silicagel column chromatography (EtOAc-hexane, a linear gradient of EtOAc from 0 to 20%) afforded 3-[(4-bromo-2-iodophenoxy)methyl]-6-chlorohex-1-en-3-ol (1.35 g).