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Isopropenyl acetate → Cholesta-1,5,7-trien-3-ol

HRID 3984
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HRID 3984 반응식
[CH3:1][CH:2]([CH2:4][CH2:5][CH2:6][C@H:7]([C@@H:9]1[C@:26]2([CH3:27])[C@H:12]([C@H:13]3[C@H:23]([CH2:24][CH2:25]2)[C@:21]2([CH3:22])[C:16](=[CH:17][C:18](=[O:28])[CH:19]=[CH:20]2)[CH:15]=[CH:14]3)[CH2:11][CH2:10]1)[CH3:8])[CH3:3].C(OC(C)=C)(=O)C.[Cl-].[Ca+2].[Cl-].[BH4-].[Na+]>CO.C(O)C.C(O)(=O)C>[CH3:3][CH:2]([CH2:4][CH2:5][CH2:6][C@H:7]([C@@H:9]1[C@:26]2([CH3:27])[C@H:12]([C:13]3[C@H:23]([CH2:24][CH2:25]2)[C@:21]2([CH3:22])[C:16]([CH2:17][CH:18]([OH:28])[CH:19]=[CH:20]2)=[CH:15][CH:14]=3)[CH2:11][CH2:10]1)[CH3:8])[CH3:1]
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참가 물질

8

반응물 4

HCID 7916Isopropenyl acetateHCID 1073901,4,6-Cholestatrien-3-oneHCID 4311764Sodium borohydrideHCID 5284359Calcium Chloride

생성물 1

HCID 18611553Cholesta-1,5,7-trien-3-ol수율 63%

시약·촉매·용매 3

HCID 176Acetic Acid
용매
HCID 702Ethanol용매
HCID 887Methanol용매

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온도
0 °C

실험 절차

To a mixture of 38 g (0.1 mol) of cholesta-1,4,6-trien-3-one and 17 g (0.1 mol) of paratoluenesulfonic acid were added 400 g (4 mol) of isopropenyl acetate, and the mixture was heated under reflux for 3 hours. The reaction solution was thoroughly washed with water until it was neutral, and dried over sodium sulfate A solution of the thus obtained concentrate in 600 ml of ether was added dropwise at a temperature of -5° C. to -10° C. to a reducer solution and stirred at 0° C. for 6 hours, said reducer solution being prepared by cooling a solution of 90 g of calcium chloride in 1,500 ml of methanol to a temperature of -5° C. to -10° C., then adding dropwise thereto a solution of 45 g of sodium borohydride in 2,000 ml of ethanol, and stirring the reaction solution at a temperature of -5° C. to -10° C. for 60 minutes. After completion of the reaction, 50% acetic acid was added to the reaction mixture and the resultant solution was extracted with ether. The ethereal layer separated was washed with water and then sodium bicarbonate solution, dried over sodium sulfate and distilled under reduced pressure to remove ether therefrom. The residue was recrystallized from acetone to yield 23.9 g of cholesta-1,5,7-trien-3-ol (IV), m.p. 126°-127° C. The yield was 63%.

후처리

  1. temperaturethe mixture was heated
  2. temperatureunder reflux for 3 hours
  3. washThe reaction solution was thoroughly washed with water until it
  4. dry with materialdried over sodium sulfate A solution of the
  5. customthus obtained
  6. concentrationconcentrate in 600 ml of ether
  7. additionwas added dropwise at a temperature of -5° C. to -10° C. to a reducer solution
  8. custombeing prepared
  9. additionadding dropwise
  10. additionwas added to the reaction mixture
  11. extractionthe resultant solution was extracted with ether
  12. customThe ethereal layer separated
  13. washwas washed with water
  14. dry with materialsodium bicarbonate solution, dried over sodium sulfate
  15. distillationdistilled under reduced pressure
  16. customto remove ether
  17. customThe residue was recrystallized from acetone

출처 및 근거

ORD 기록
ord-0ef1704cd51e4103bf0c70a5c34931c8
출처 데이터셋
uspto-grants-1988_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04723045

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