反応式
Cl[C:2]1[CH:11]=[CH:10][C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[N:3]=1.[CH:12]1([Mg]Br)[CH2:16][CH2:15][CH2:14][CH2:13]1>C(OCC)C.[Cl-].[NH4+].C1C=CC(P(C2C=CC=CC=2)CCP(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.Cl[Ni]Cl>[CH:12]1([C:2]2[CH:11]=[CH:10][C:9]3[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=3)[N:3]=2)[CH2:16][CH2:15][CH2:14][CH2:13]1参加物
反応条件
- 温度
- 0 °C
実験手順
To a solution of 2-chloroquinoline (8.2 g, 50 mmol) and [1,2-bis(diphenylphosphino)-ethane]dichloronickel(II) (200 mg, 0.38 mmol) in diethyl ether (20 ml) cooled in a ice/methanol bath was added cyclopentylmagnesium bromide (2 M solution in diethyl ether; 25.5 ml, 51 mmol) over a period of 15 minutes. The resulting brown solution was then stirred for 30 minutes, the ice bath removed and the mixture stirred for a further 10 minutes. The reaction mixture was then re-cooled to 0° C. and a saturated ammonium chloride solution (40 ml) added slowly. The resulting reaction mixture was poured into a separating funnel and further diluted with diethyl ether (60 ml) and saturated ammonium chloride solution (60 ml). The organics were separated and the aqueous layer washed with diethyl ether (2×100 ml). The combined organics were dried (MgSO4), filtered and the solvent removed in vacuo to leave 2-cyclopentylquinoline (9.98 g, 50.4 mmol) as an oil.
後処理
- customthe ice bath removed
- stirringthe mixture stirred for a further 10 minutes
- additiona saturated ammonium chloride solution (40 ml) added slowly
- customThe resulting reaction mixture
- additionwas poured into a separating funnel
- customThe organics were separated
- washthe aqueous layer washed with diethyl ether (2×100 ml)
- dry with materialThe combined organics were dried (MgSO4)
- filtrationfiltered
- customthe solvent removed in vacuo
出典と根拠
- ORDレコード
- ord-6ef299c453e641a5a40b6ddbf30a612a
- 出典データセット
- uspto-grants-2010_08
- 特許番号
- US07772227B2
関連ノート
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