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Sodium Iodide → 4-Methoxy-4-(3-iodo-trans-propenyl)tetrahydropyran

HRID 1757449
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HRID 1757449 반응식
[CH3:1][O:2][C:3]1(/[CH:9]=[CH:10]/[CH2:11]S(C)(=O)=O)[CH2:8][CH2:7][O:6][CH2:5][CH2:4]1.[Na+].[I-:17]>CC(C)=O>[CH3:1][O:2][C:3]1(/[CH:9]=[CH:10]/[CH2:11][I:17])[CH2:8][CH2:7][O:6][CH2:5][CH2:4]1
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참가 물질

4

반응물 2

HCID 5238Sodium IodideHCID 193880264-Methoxy-4-(3-methanesulfonyl-trans-prop-1-enyl)tetrahydropyran

생성물 1

HCID 152840384-Methoxy-4-(3-iodo-trans-propenyl)tetrahydropyran수율 97.1%

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

To a 0° C. solution in acetone of 4-methoxy-4-(3-methanesulfonyl-trans-prop-1-enyl)tetrahydropyran (730 mg, 2.92 mmol), prepared as in step 5, was added NaI (5.84 mmol, 875 mg). The cold bath was removed and the reaction mixture was stirred for 2 hours at ambient temperature. The reaction mixture was then concentrated and the residue partitioned between ether and H2O. The organic phase was washed twice with brine, dried over MgSO4, decolorized with activatedcarbon, filtered, through a pad of celite and concentrated in vacuo. The 4-methoxy-4-(3-iodo-trans -prop-1-enyl)tetrahydropyran (800 mg) so obtained was used without further purification.

후처리

  1. customThe cold bath was removed
  2. concentrationThe reaction mixture was then concentrated
  3. customthe residue partitioned between ether and H2O
  4. washThe organic phase was washed twice with brine
  5. dry with materialdried over MgSO4
  6. filtrationfiltered, through a pad of celite
  7. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-8ede66db32554691b5bd76ea89c64b36
출처 데이터셋
uspto-grants-1995_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05446062

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