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
- 40 °C
PROCEDURE
实验过程
95% Sodium hydride (40.85 g, 1.6 moles) was placed into a 3 L flask under argon and THF (1.2 L) at −10° C. was added. Dry tetraethylene glycol (500.0 g, 2.57 moles) was added slowly. The pot temperature was maintained below 15° C. during the addition. Once the NaH had reacted, a homogeneous solution resulted. 18C6 (3.9 g) and dimethyl-acetamide (DMAC, 500 mL) was added. Chloroisodurene (TMB-Cl, 98.6 g, 0.58 mole) dissolved in THF (500 mL) was added to pot over about 4 h. The reaction mixture was stirred for about 17 h at about 40° C. under argon. The reaction was monitored by tlc on silica gel plates, eluting with 10% MeOH/CH2Cl2 vs TMB-Cl. The reaction was complete; the TMB-Cl was consumed. The solvent was removed in vacuo; the resulting oil was extracted with CH2Cl2 (700 mL) and water (300 mL). The CH2Cl2 layer was separated, dried over MgSO4, filtered through fluted filter paper and concentrated in vacuo to leave an oil. A column was prepared with 600 g of silica gel and hexane as needed. The crude product was placed onto column with hexane and a minimum of t-butylmethyl ether (TBME, 100 mL) to make a clean transfer. The column was eluted with hexane (4 L) and then as follows: (2 L) 10% TBME/hexane; (2 L) 20% TBME/hexane; (4 L) TBME/hexane; (3 L) 40% TBME/hexane, and (2 L) TBME. Like fractions containing product were combined and concentrated in vacuo to give 140.2 g (73%). The product was characterized by nmr. 1H NMR[400 MHz, DMSO(d6)] □6.81 (s, 2H), 4.56 (t, 1H), 4.45 (s, 2H), 3.57-3.45 (m, 14H), 3.41 (t, 2H), 2.28 (s, 6H), 2.22 (s, 3H).
WORKUP
后处理
- temperatureThe pot temperature was maintained below 15° C. during the addition
- customa homogeneous solution resulted
- additionwas added to pot over about 4 h
- washeluting with 10% MeOH/CH2Cl2 vs TMB-Cl
- customthe TMB-Cl was consumed
- customThe solvent was removed in vacuo
- extractionthe resulting oil was extracted with CH2Cl2 (700 mL) and water (300 mL)
- customThe CH2Cl2 layer was separated
- dry with materialdried over MgSO4
- filtrationfiltered
- filtrationthrough fluted filter paper
- concentrationconcentrated in vacuo
- customto leave an oil
- washThe column was eluted with hexane (4 L)
- additionLike fractions containing product
- concentrationconcentrated in vacuo
- customto give 140.2 g (73%)