تفاعل #215283

معادلة التفاعل

hydrogen chloride

3-benzoyloxy-1,2,3,4-tetrahydrocarbazole

sodium hydride

3-benzoyloxy-1,2,3,4-tetrahydrocarbazole hydrochloride

3-(dimethylamino)propyl chloride

→

3-benzoyloxy-9-[3-(dimethylamino)propyl]-1,2,3,4-tetrahydrocarbazole

المذيبات

dimethylformamide

ظروف التفاعل

المعالجة

1. 1
   استخلاصThe crude free base was extracted from the water
2. 2
   workup.ADDITIONdiluted
3. 3
   أخرىreaction mixture into ether
4. 4
   أخرىThe resulting precipitate was recrystallized from isopropyl alcohol and ethyl acetate
5. 5
   أخرىto give 6.2 g

الإجراء التجريبي

The 3-benzoyloxy-9-[3-(dimethylamino)propyl]-1,2,3,4-tetrahydrocarbazole was prepared by following an alkylation procedure similar to that described in Example 11 and using 29.1 g. of 3-benzoyloxy-1,2,3,4-tetrahydrocarbazole and 4.3 g. of sodium hydride (50% in mineral oil) in 200 ml. of dimethylformamide, and 13 g. of 3-(dimethylamino)propyl chloride. The crude free base was extracted from the water diluted reaction mixture into ether and the ethereal solution was treated with ethereal hydrogen chloride. The resulting precipitate was recrystallized from isopropyl alcohol and ethyl acetate to give 6.2 g. of 3-benzoyloxy-1,2,3,4-tetrahydrocarbazole hydrochloride, m.p. 162°-180° C.

المصدر