반응 #51657

ord-a65b2e5f84f64afcafd49ee0a267d32c

반응 조건

온도
-10°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타was replaced by a dry-ice acetone bath
  2. 2
    기타was lowered to −50° C
  3. 3
    workup.STIRRINGwith stirring
  4. 4
    workup.STIRRINGThe reaction mixture was stirred
  5. 5
    workup.WAITto reach 20° C. over about an hour
  6. 6
    workup.STIRRINGwith stirring
  7. 7
    기타the precipitate which formed
  8. 8
    여과was filtered
  9. 9
    세척washed well with ether
  10. 10
    기타dried overnight in a vacuum oven at room temperature

실험 절차

N-chlorosuccinimide (3.85 g, 29.35 mmole) was suspended in dichloroethane (40 ml) under a nitrogen atmosphere and cooled to −10° C. using an ice-salt-acetone bath. Dimethylsulfide (3 ml) was slowly added with stirring over a period of about 5 minutes. The mixture was stirred at this temperature for 10 minutes beyond the addition, at which time the ice-salt-acetone bath was replaced by a dry-ice acetone bath and the temperature was lowered to −50° C. To this solution was added 2-methylindole (3.85 g, 29.35 mmole) dissolved in dichloroethane (40 ml) slowly with stirring. The reaction mixture was stirred while allowing the temperature to reach 20° C. over about an hour. Diethyl ether (90 ml) was added with stirring and the precipitate which formed was filtered, washed well with ether, and dried overnight in a vacuum oven at room temperature. The free-flowing powder of (2-methyl-1H-indol-3-yl)-dimethylsulfonium chloride thus obtained was used without further purification in the following step.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US06852726B2uspto-grants-2005_02