反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
CONDITIONS
反应条件
- 温度
- -78 °C
PROCEDURE
实验过程
BuLi (1.55 M in hexane, 14.7 mL, 22.7 mmol) was added to a sol. of 1-bromo-2-(dimethoxymethyl)benzene (5.00 g, 21.6 mmol) in Et2O (50 mL). The mixture was stirred for 30 min at −78 ° C. and MgBr2.Et2O (5.87 g, 22.7 mmol) was added. The mixture was allowed to warm up to 0° C. over 15 min and CuI (420 mg, 2.16 mmol) was added. The mixture was stirred at 0° C. for 5 min and allyl bromide (1.92 mL, 22.7 mmol) was added. The mixture was stirred overnight while warming up to rt. Aq. 1M HCl (1 mL) was added and the mixture was diluted with Et2O, and washed with aq. 1M HCl (1×). The org. Extracts were dried over MgSO4, filtered, and the solvents were removed under reduced pressure. The residue was dissolved in acetone (20 mL) and water (10 mL), and TosOH (cat. amount) was added. The mixture was stirred for 5 h at rt, and the solvents were partially removed under reduced pressure. The residue was diluted with Et2O, and washed with aq. 1M HCl (1×), and aq. sat. NaHCO3 (1×). The org. extracts were dried over MgSO4, filtered, and the solvents were removed under reduced pressure. Purification of the residue by FC (Et2O/petroleum ether 1:49→24:1) yielded 2-allylbenzaldehyde (1.06 g, 34%). This compound was transformed into the title compound following typical procedure J with cyclopropylamine.
WORKUP
后处理
- temperatureto warm up to 0° C. over 15 min
- stirringThe mixture was stirred at 0° C. for 5 min
- stirringThe mixture was stirred overnight
- temperaturewhile warming up to rt
- washwashed with aq. 1M HCl (1×)
- dry with materialExtracts were dried over MgSO4
- filtrationfiltered
- customthe solvents were removed under reduced pressure
- dissolutionThe residue was dissolved in acetone (20 mL)
- additionwater (10 mL), and TosOH (cat. amount) was added
- stirringThe mixture was stirred for 5 h at rt
- customthe solvents were partially removed under reduced pressure
- additionThe residue was diluted with Et2O
- washwashed with aq. 1M HCl (1×), and aq. sat. NaHCO3 (1×)
- dry with materialextracts were dried over MgSO4
- filtrationfiltered
- customthe solvents were removed under reduced pressure
- customPurification of the residue by FC (Et2O/petroleum ether 1:49→24:1)