Tetrahydrofuran → [4-(3-Hydroxypentan-3-yl)-2-methylphenyl]boronic acid
反応式
Br[C:2]1[CH:7]=[CH:6][C:5]([C:8]([OH:13])([CH2:11][CH3:12])[CH2:9][CH3:10])=[CH:4][C:3]=1[CH3:14].O1CCCC1.C([Li])CCC.[B:25](OC(C)C)([O:30]C(C)C)[O:26]C(C)C>CCCCCC>[CH2:9]([C:8]([C:5]1[CH:6]=[CH:7][C:2]([B:25]([OH:30])[OH:26])=[C:3]([CH3:14])[CH:4]=1)([OH:13])[CH2:11][CH3:12])[CH3:10]参加物
反応条件
- 温度
- -70 °C
実験手順
In a three-necked flask, introduce under nitrogen 5 g of 3-(4-bromo-3-methylphenyl)pentan-3-ol (19.4 mmol) and 50 cm3 of tetrahydrofuran. Cool the mixture to −70° C. and add dropwise 23.3 cm3 (58 mmol) of a 2.5M solution of n-butyllithium in hexane, over 30 minutes. Leave the mixture for approximately 2 h with stirring at −70° C. and then add dropwise 13.5 cm3 of triisopropyl borate (58 mmol), over 20 minutes. Leave the mixture with stirring for 3 h, allowing the temperature to increase to −10° C. Hydrolyse the mixture with saturated NH4Cl solution and extract two times with ethyl acetate. Wash the combined organic phases with saturated sodium chloride solution and dry them over sodium sulfate. Evaporate the solvents under vacuum. This gives 5 g of a colorless oil, which is chromatographed on silica gel (heptane/ethyl acetate=9/1) to give 4-(1-ethyl-1-hydroxypropyl)-2-methylphenylboronic acid in the form of a highly viscous oil. (Yield=71%)
後処理
- customLeave the mixture for approximately 2 h
- waitover 20 minutes
- customLeave the mixture
- stirringwith stirring for 3 h
- temperatureto increase to −10° C
- extractionHydrolyse the mixture with saturated NH4Cl solution and extract two times with ethyl acetate
- washWash the combined organic phases with saturated sodium chloride solution
- dry with materialdry them over sodium sulfate
- customEvaporate the solvents under vacuum
- customThis gives 5 g of a colorless oil, which is chromatographed on silica gel (heptane/ethyl acetate=9/1)
出典と根拠
- ORDレコード
- ord-aea31dcd9fb0419facdcf05b3aeedaba
- 出典データセット
- uspto-grants-2010_02
- 特許番号
- US07659421B2
反応ノート
読み込み中…