Butanal, 4-[(tetrahydro-2H-pyran-2-yl)oxy]- → 2-{[5-(4-Chlorophenyl)pent-4-en-1-yl]oxy}oxane

HRID 1381368

반응식

HRID 1381368 반응식
C([Li])CCC.[Cl-].[Cl:7][C:8]1[CH:33]=[CH:32][C:11]([CH2:12][P+](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=[CH:10][CH:9]=1.[O:34]1[CH2:39][CH2:38][CH2:37][CH2:36][CH:35]1[O:40][CH2:41][CH2:42][CH2:43][CH:44]=O>O1CCCC1>[Cl:7][C:8]1[CH:9]=[CH:10][C:11]([CH:12]=[CH:44][CH2:43][CH2:42][CH2:41][O:40][CH:35]2[CH2:36][CH2:37][CH2:38][CH2:39][O:34]2)=[CH:32][CH:33]=1

참가 물질

5

실험 절차

In an argon atmosphere, butyllithium (10%; 37 ml) was added dropwise to a suspension of (4-chlorobenzyl)triphenylphosphonium chloride (24 g) in tetrahydrofuran (70 ml) with ice-cooling and stirring. After stirring at the same temperature for 30 minutes, a solution of 4-tetrahydropyranyloxy-1-butanal (9 g) in tetrahydrofuran (30 ml) was added dropwise, and the mixture was stirred at room temperature for 2 hours. The tetrahydrofuran was distilled off under reduced pressure and water was added to the residue, followed by extraction with petroleum ether. After washing with water and drying over magnesium sulfate, the solvent was distilled off, and the residue was subjected to silica gel column chromatography, elution being carried out with chloroform to give 1-(4-chlorophenyl)-5-(2-tetrahydropyranyloxy)-1-pentene (7 g) as a light-yellow oil.

후처리

  1. temperaturecooling
  2. stirringAfter stirring at the same temperature for 30 minutes
  3. stirringthe mixture was stirred at room temperature for 2 hours
  4. distillationThe tetrahydrofuran was distilled off under reduced pressure and water
  5. additionwas added to the residue
  6. extractionfollowed by extraction with petroleum ether
  7. washAfter washing with water
  8. dry with materialdrying over magnesium sulfate
  9. distillationthe solvent was distilled off
  10. washthe residue was subjected to silica gel column chromatography, elution

출처 및 근거

ORD 기록
ord-a1407fe3feb24b278729b8e8236e9ebe
출처 데이터셋
uspto-grants-1986_04
특허 번호
US04585789

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