Chlorotrimethylsilane → Silane, (10-bromo-9-anthracenyl)trimethyl-

HRID 902404

반응식

HRID 902404 반응식
[Br:1][C:2]1[C:3]2[C:8]([C:9](Br)=[C:10]3[C:15]=1[CH:14]=[CH:13][CH:12]=[CH:11]3)=[CH:7][CH:6]=[CH:5][CH:4]=2.C([Li])(C)(C)C.Cl[Si:23]([CH3:26])([CH3:25])[CH3:24]>C1COCC1>[Br:1][C:2]1[C:3]2[C:8]([C:9]([Si:23]([CH3:26])([CH3:25])[CH3:24])=[C:10]3[C:15]=1[CH:14]=[CH:13][CH:12]=[CH:11]3)=[CH:7][CH:6]=[CH:5][CH:4]=2

참가 물질

5

반응 조건

온도
-69 °C

실험 절차

Under an argon atmosphere, the temperature of a solution of 9,10-dibromoanthracene (5 g, 15 mmol) in dry-THF (50 ml) was cooled to −69° C., and t-butyllithium (18 mmol) was dropped to the solution. After the mixture had been stirred for 3 hours, chlorotrimethylsilane (3 ml, 22.5 mmol) was added to the mixture, and the whole was stirred at −69° C. for an additional 3 hours. After the temperature of the resultant had been increased to room temperature, the resultant was quenched with sodium bicarbonate water, extracted with toluene, and dried with sodium sulfate. Then, the solvent was removed by distillation. The residue was dispersed and washed with hexane, the insoluble matter was removed, and the filtrate was condensed. The condensate was washed with ethanol, and was then subjected to silica gel column chromatography, whereby 1 g of 9-bromo-10-trimethylsilylanthracene was obtained.

후처리

  1. stirringthe whole was stirred at −69° C. for an additional 3 hours
  2. temperatureAfter the temperature of the resultant had been increased to room temperature
  3. customthe resultant was quenched with sodium bicarbonate water
  4. extractionextracted with toluene
  5. dry with materialdried with sodium sulfate
  6. customThen, the solvent was removed by distillation
  7. additionThe residue was dispersed
  8. washwashed with hexane
  9. customthe insoluble matter was removed
  10. customcondensed
  11. washThe condensate was washed with ethanol

출처 및 근거

ORD 기록
ord-1149d602c24b4fc49eafb64fecc366d4
출처 데이터셋
uspto-grants-2008_04
특허 번호
US07365198B2

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