Sodium hydride → 2-(3-Cyano-3-(3,4-dichlorophenyl)propyl)oxytetrahydropyran

HRID 355465

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HRID 355465 반응식
[Cl:1][C:2]1[CH:3]=[C:4]([CH2:9][C:10]#[N:11])[CH:5]=[CH:6][C:7]=1[Cl:8].[H-].[Na+].Br[CH2:15][CH2:16][O:17][CH:18]1[CH2:23][CH2:22][CH2:21][CH2:20][O:19]1.[Cl-].[NH4+]>C1COCC1.O>[Cl:1][C:2]1[CH:3]=[C:4]([CH:9]([CH2:15][CH2:16][O:17][CH:18]2[CH2:23][CH2:22][CH2:21][CH2:20][O:19]2)[C:10]#[N:11])[CH:5]=[CH:6][C:7]=1[Cl:8]

참가 물질

7

실험 절차

A solution of 100 g of 3,4-dichlorophenylacetonitrile in 500 ml of THF is added dropwise at 20° C. over 30 minutes to a suspension of 16.5 g of sodium hydride in 200 ml of dry THF, and the reaction mixture is then stirred at RT for 2 hours. It is cooled to -20° C., a solution of 118 g of 1-bromo-2-(tetrahydro-2-pyranyloxy)ethane in 100 ml of THF is added and the mixture is left stirring for 2 hours while allowing the temperature to rise to RT. A solution of 50 g of ammonium chloride in 3 liters of water is then added, the product is extracted with 1.5 liters of ether, and the organic phase is washed with saturated sodium chloride solution, dried over magnesium sulphate and evaporated under vacuum. The residue is chromatographed on silica, eluting with DCM and then with a DCM/AcOEt (95:5; v/v) mixture. 118 g of the expected product are obtained in the form of an oil.

후처리

  1. temperatureIt is cooled to -20° C.
  2. waitthe mixture is left
  3. stirringstirring for 2 hours
  4. customto rise to RT
  5. extractionthe product is extracted with 1.5 liters of ether
  6. washthe organic phase is washed with saturated sodium chloride solution
  7. dry with materialdried over magnesium sulphate
  8. customevaporated under vacuum
  9. customThe residue is chromatographed on silica
  10. washeluting with DCM

출처 및 근거

ORD 기록
ord-b1d7c9ccde3b4fbcb2f25e47e0f86004
출처 데이터셋
uspto-grants-1998_11
특허 번호
US05830906

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