반응 #702829

반응 방정식

potassium hydroxide

β-chloroethyltoluenesulfonate

sodium hydroxide

potassium hydroxide

3-bromo-9-(2-chloroethyl)-carbazole

β-chloroethyltoluenesulfonate

sodium hydroxide

3-Bromo-9-vinylcarbazole 3-Bromocarbazole

→

3-bromo-9-vinylcarbazole

수율 95.0%

용매

ethanol

water

water

diethyl ether

tetrahydrofuran

acetone

반응 조건

후처리

1. 1
   온도to reflux
2. 2
   온도Refluxing
3. 3
   기타was formed in >95 percent yield
4. 4
   세척washed successively with two 150 ml portions of distilled water and 100 ml saturated sodium chloride solution
5. 5
   기타The organic phase was separated
6. 6
   건조dried over sodium sulfate
7. 7
   여과filtered
8. 8
   기타Solvents were removed on a rotary evaporator at reduced pressure
9. 9
   workup.DISSOLUTIONThe crude 3-bromo-9-(2-chloroethyl)carbazole was dissolved in 230 ml isopropanol
10. 10
    workup.ADDITIONwas added
11. 11
    온도The resulting solution was refluxed for 11/2 hours
12. 12
    온도refluxing
13. 13
    기타2 hours
14. 14
    온도The solution was cooled in a freezer during which time a solid residue
15. 15
    기타formed
16. 16
    여과After filtration
17. 17
    세척the solid was washed with water
18. 18
    기타Recrystallization from methanol

실험 절차

3-Bromo-9-vinylcarbazole-3-Bromocarbazole (24.6 g, 0.1 mole) was dissolved in acetone. To it was added β-chloroethyltoluenesulfonate (31.68 g, 0.135 moles) and sodium hydroxide (13 g, 0.325 mole) dissolved in 10 ml of distilled water. The mixture was brought to reflux. After 24 hours, equal amounts of β-chloroethyltoluenesulfonate, sodium hydroxide, and water were added. Refluxing was continued until 3-bromo-9-(2-chloroethyl)-carbazole was formed in >95 percent yield as judged by GLPC analysis. The product was dissolved in a mixture of 250 ml diethyl ether and tetrahydrofuran (50:50 v/v) and washed successively with two 150 ml portions of distilled water and 100 ml saturated sodium chloride solution. The organic phase was separated and dried over sodium sulfate and filtered. Solvents were removed on a rotary evaporator at reduced pressure. The crude 3-bromo-9-(2-chloroethyl)carbazole was dissolved in 230 ml isopropanol. 8.4 g (0.15 mole) potassium hydroxide dissolved in 15 ml ethanol was added. The resulting solution was refluxed for 11/2 hours. 4.2 g of solid potassium hydroxide was then added, and refluxing was continued for an additional 11/2 hours. The solution was cooled in a freezer during which time a solid residue formed. After filtration, the solid was washed with water. Recrystallization from methanol gave 13.94 g 3-bromo-9-vinylcarbazole as pale yellow-white needles (mp 74-74.5 degrees Celsius).

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