Water → Methyl 4-[(phenylmethylene)amino]-6-(trimethylsilyl)-5-hexynoate

HRID 1380485노트

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HRID 1380485 반응식
C([Li])CCC.[CH:6](=[N:13][CH2:14][C:15]#[C:16][Si:17]([CH3:20])([CH3:19])[CH3:18])[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1.[C:21]([O:25][CH3:26])(=[O:24])[CH:22]=[CH2:23].O>CCCCCC.O1CCCC1>[CH3:20][Si:17]([CH3:19])([CH3:18])[C:16]#[C:15][CH:14]([N:13]=[CH:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1)[CH2:23][CH2:22][C:21]([O:25][CH3:26])=[O:24]

참가 물질

7

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온도
-70 °C

실험 절차

53.6 ml of a 1.6M solution of n-butyllithium in hexane was added drop-by-drop over 20 minutes to a solution of 18.0 g of 1B in 700 ml of dry tetrahydrofuran at -70° C. The resulting mixture was stirred for 20 minutes at -70° C., when 7.2 g of freshly distilled methyl acrylate was added over 14 minutes. The resulting mixture was stirred for 30 minutes at -70° C., when 16.5 ml of water was added drop-by-drop. The resulting mixture was allowed to warm slowly to room temperature; the solvent was evaporated; the residue was diluted with water and the resulting mixture was extracted with ether. The ether extract was washed with brine, dried (Na2SO4), filtered and the solvent was evaporated. The residue (a dark thick oil) was distilled in a Kugelrohr apparatus to give methyl 6-(trimethylsilyl)-4-(benzylideneamino)-5-hexynoate (3A), b.p.: 140°-142° C. (0.01 Torr.).

후처리

  1. stirringThe resulting mixture was stirred for 30 minutes at -70° C.
  2. temperatureto warm slowly to room temperature
  3. customthe solvent was evaporated
  4. additionthe residue was diluted with water
  5. extractionthe resulting mixture was extracted with ether
  6. extractionThe ether extract
  7. washwas washed with brine
  8. dry with materialdried (Na2SO4)
  9. filtrationfiltered
  10. customthe solvent was evaporated
  11. distillationThe residue (a dark thick oil) was distilled in a Kugelrohr apparatus

출처 및 근거

ORD 기록
ord-e11d15204bd94fcfb6e119ee36644b5a
출처 데이터셋
uspto-grants-1986_04
특허 번호
US04582529

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