반응 #335791

반응 방정식

potassium hydroxide

potassium hydroxide

bis(2-mercaptoethyl)ether

p-Vinylbenzyl chloride

2-bromoethanol

→

solid

수율 43.7%

2-{2-[2-(4-vinylbenzylthio)ethoxy]ethylthio}ethanol

수율 43.7%

용매

ethanol

반응 조건

후처리

1. 1
   workup.STIRRINGstirring
2. 2
   workup.WAITwas continued at ambient temperature for 30 minutes
3. 3
   workup.STIRRINGagain stirring
4. 4
   workup.WAITwas continued at ambient temperature for 30 minutes
5. 5
   workup.STIRRINGstirred at room temperature for 16 hours
6. 6
   여과The next day the reaction was filtered
7. 7
   기타the solvent removed on a rotary evaporator
8. 8
   workup.ADDITIONTo the residue was added dichloromethane (1.2 liter)
9. 9
   세척the mixture was washed with water (200 ml), 5% hydrochloric acid (200 ml), saturated sodium chloride (200 ml)
10. 10
    건조then dried over anhydrous magnesium sulfate
11. 11
    여과filtered
12. 12
    기타the solvent removed in a rotary evaporator
13. 13
    workup.ADDITIONTo the residue was added diethyl ether (350 ml) and hexane (200 ml)
14. 14
    온도the mixture was cooled in the freezer
15. 15
    여과filtered

실험 절차

To a solution of potassium hydroxide (48 g, 0.72 molar) in ethanol (1 liter) was added bis(2-mercaptoethyl)ether (100 g, 0.72 moles) and the mixture was stirred for 30 minutes at ambient temperature. Then 2-bromoethanol (90 g, 0.72 mole) was added to the mixture all at once and stirring was continued at ambient temperature for 30 minutes, then potassium hydroxide (48.0 g, 0.72 mole) was added to the mixture and again stirring was continued at ambient temperature for 30 minutes. p-Vinylbenzyl chloride (110 g, 0.72 mole) was then added all at once and stirred at room temperature for 16 hours. The next day the reaction was filtered and the solvent removed on a rotary evaporator. To the residue was added dichloromethane (1.2 liter), the mixture was washed with water (200 ml), 5% hydrochloric acid (200 ml), saturated sodium chloride (200 ml) then dried over anhydrous magnesium sulfate, filtered and the solvent removed in a rotary evaporator. To the residue was added diethyl ether (350 ml) and hexane (200 ml) and then the mixture was cooled in the freezer, filtered to give a white solid (94 g). Chromatography on the mother liquors gave additional product (48 g). Yield of 66%. Analysis calculated for C15H22O2S2. C, 60.36, H, 7.43, S, 21.49. Found: C, 60.41, H, 7.43, S, 21.14. 1H NMR (CDCl3) δ 2.7 (m, 6H, CH2S--CH2 +SCH2), 3.0-3.8 (m, 9H, ArCH2S, CH2OCH2,CH2OH), 5.15+5.65 (AB quartet, 2H, CH2 =), 6.68 (m, 1H, CH=), 7.25 (m, 4H, ArH's).

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