تفاعل #1836420

معادلة التفاعل

1-chloro-2-(2-methoxyethoxy)ethane

carbazole

NaH

→

alkylated carbazole

المردود 83.0%

9-(2-(2-methoxyethoxy)ethyl)-9H-carbazole

المردود 83.0%

المذيبات

DMF

ظروف التفاعل

المعالجة

1. 1
   درجة الحرارةAfter cooling down to 0° C.
2. 2
   أخرىthe reaction mixture was carefully quenched with water
3. 3
   استخلاصextracted with ethyl acetate three times
4. 4
   غسيلThe combined organic phase was washed with water and brine
5. 5
   تجفيفThen the organic layer was dried over anhydrous sodium sulfate
6. 6
   أخرىthe solvent was removed
7. 7
   أخرىThe residue was purified by silica gel chromatography

الإجراء التجريبي

To a solution of carbazole (3.34 g, 20 mmol) in DMF (80 mL) at 0° C. was added NaH (0.72 g, 30 mmol). After heating to 80° C. for 1.5 h, 1-chloro-2-(2-methoxyethoxy)ethane (3.31 g, 24 mmol) was added dropwise. The resulting mixture was kept at 80° C. overnight. After cooling down to 0° C., the reaction mixture was carefully quenched with water and extracted with ethyl acetate three times. The combined organic phase was washed with water and brine. Then the organic layer was dried over anhydrous sodium sulfate and the solvent was removed. The residue was purified by silica gel chromatography using petroleum ether and ethyl acetate as eluent (EA:PE=1:3) to afford alkylated carbazole 1a (4.46 g) as brown oil in 83% yield. 1H NMR (400 MHz, CDCl3) δ 8.09 (d, J=7.6 Hz, 2H), 7.46 (m, 4H), 7.23 (m, 2H), 4.51 (t, J=6.4 Hz, 2H), 3.86 (t, J=6.4 Hz, 2H), 3.52 (m, 2H), 3.42 (m, 2H), 3.31 (s, 3H). 13C NMR (400 MHz, CDCl3) δ 140.5, 125.6, 122.8, 120.2, 118.9, 108.7, 71.8, 70.7, 69.1, 59.0, 43.0. MS (FAB) m/z Calcd for C17H19NO2 269.1. Found 269.2 [M]+.

المصدر