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
- 0 °C
PROCEDURE
实验过程
A cold (5° C.) solution of (1S,2R)-1-amino-2-indanol (400 mg, 2.68 mmol) in THF (160 mL) was added dropwise to a cold (0° C.) solution of borane-diethylaniline complex (7.0 g, 43 mmol) in THF (20 mL). After complete addition, the resulting solution was stirred at (0° C.) for 30 min then 2-bromo-4′-benzyloxy-3′-nitroacetophenone (20.0 g, 57.1 mmol) was added in three portions over a 30 min period. The resulting solution was stirred at <5° C. for 1 h, quenched by dropwise addition of acetone (17 mL) then allowed to warm to ambient temperature overnight. The reaction mixture was concentrated in vacuo to a residue, which was dissolved in toluene (100 mL) and washed in succession with 10% H2SO4 (2×45 mL), H2O (2×45 mL) and sat. brine (1×40 mL). The organic layer was dried over MgSO4, clarified then concentrated in vacuo to a volume of ˜40 mL. Heptane (45 mL) was slowly added to give a thick slurry. The solid was collected on a filter and washed with heptane (2×5 mL). This material was dissolved in warm toluene (˜50 mL), the solution was clarified then diluted with heptane (50 mL). The resulting mixture was stirred for 30 min, the solids were collected, washed with heptane (2×5 mL) then dried to constant weight in vacuo to give 18.9 g (94.0%) of the title compound.
WORKUP
后处理
- additionAfter complete addition
- stirringThe resulting solution was stirred at <5° C. for 1 h
- customquenched by dropwise addition of acetone (17 mL)
- temperatureto warm to ambient temperature overnight
- concentrationThe reaction mixture was concentrated in vacuo to a residue, which
- dissolutionwas dissolved in toluene (100 mL)
- washwashed in succession with 10% H2SO4 (2×45 mL), H2O (2×45 mL) and sat. brine (1×40 mL)
- dry with materialThe organic layer was dried over MgSO4
- concentrationclarified then concentrated in vacuo to a volume of ˜40 mL
- additionHeptane (45 mL) was slowly added
- customto give a thick slurry
- customThe solid was collected on
- filtrationa filter
- washwashed with heptane (2×5 mL)
- dissolutionThis material was dissolved in warm toluene (˜50 mL)
- additionthe solution was clarified then diluted with heptane (50 mL)
- stirringThe resulting mixture was stirred for 30 min
- customthe solids were collected
- washwashed with heptane (2×5 mL)
- customthen dried to constant weight in vacuo