Water → 4-(4-Phenyl-4-n-pentyl-4-silacyclohexyl)cyclohexane carbaldehyde

HRID 2658

반응식

HRID 2658 반응식
C[C:2](C)([O-:4])C.[K+].[Cl-].COC[P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.[CH2:30]([Si:35]1([C:48]2[CH:53]=[CH:52][CH:51]=[CH:50][CH:49]=2)[CH2:40][CH2:39][CH:38]([CH:41]2[CH2:46][CH2:45][C:44](=O)[CH2:43][CH2:42]2)[CH2:37][CH2:36]1)[CH2:31][CH2:32][CH2:33][CH3:34].O>C1COCC1>[CH2:30]([Si:35]1([C:48]2[CH:53]=[CH:52][CH:51]=[CH:50][CH:49]=2)[CH2:36][CH2:37][CH:38]([CH:41]2[CH2:46][CH2:45][CH:44]([CH:2]=[O:4])[CH2:43][CH2:42]2)[CH2:39][CH2:40]1)[CH2:31][CH2:32][CH2:33][CH3:34]

참가 물질

6

실험 절차

12 g of potassium t-butoxide was added to a mixture of 35 g of methoxymethyltriphenylphosphonium chloride and 200 ml of THF to prepare an orange ylide solution. A solution of 34 g of 4-(4-n-pentyl-4-phenyl-4-silacyclohexyl)cyclohexanone in 50 ml of THF was added to the ylide solution and agitated at room temperature for 2 hours. Thereafter, the mixture was poured into iced water and extracted with methylene chloride, followed by washing, drying and concentration by a usual manner. n-Hexane was added to the residue, and the resultant crystals of triphenylphosphine oxide were removed by filtration. The filtrate was concentrated, and the resultant residue was hydrolyzed with 100 ml of 20% hydrochloric acid, followed by washing, drying and concentration by a usual manner to obtain 4-(4-n-pentyl-4-phenyl-4-silacyclohexyl)cyclohexane carbaldehyde.

후처리

  1. customto prepare an orange ylide solution
  2. extractionextracted with methylene chloride
  3. washby washing
  4. customdrying
  5. concentrationconcentration by a usual manner
  6. additionn-Hexane was added to the residue
  7. customthe resultant crystals of triphenylphosphine oxide were removed by filtration
  8. concentrationThe filtrate was concentrated
  9. washby washing
  10. customdrying
  11. concentrationconcentration by a usual manner

출처 및 근거

ORD 기록
ord-60ff9b3f88b74fb89fc2c3b2f2e968f6
출처 데이터셋
uspto-grants-1998_03
특허 번호
US05730901

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