Methyl iodide → 2,3-Dihydro-4-hydroxy-7-methoxy-4-methyl-4H-1-benzopyran

HRID 1732751노트

반응식

HRID 1732751 반응식
[CH3:1]I.[Mg].[CH3:4][O:5][C:6]1[CH:16]=[CH:15][C:9]2[C:10](=[O:14])[CH2:11][CH2:12][O:13][C:8]=2[CH:7]=1.[Cl-].[NH4+]>CCOCC>[OH:14][C:10]1([CH3:1])[C:9]2[CH:15]=[CH:16][C:6]([O:5][CH3:4])=[CH:7][C:8]=2[O:13][CH2:12][CH2:11]1

참가 물질

6

반응물 4

HCID 6328Methyl iodideHCID 25517Ammonium ChlorideHCID 43875107-methoxy-3,4-dihydro-2H-1-benzopyran-4-oneHCID 5462224Magnesium

생성물 1

HCID 203045882,3-Dihydro-4-hydroxy-7-methoxy-4-methyl-4H-1-benzopyran

시약·촉매·용매 1

HCID 3283Diethyl Ether용매3회

실험 절차

Methyl iodide (145 g; 64.2 ml) in dry ether (50 ml) was added dropwise with stirring to magnesium turnings (22 g) in dry ether (730 ml). After the initial reaction had ceased the reaction mixture was refluxed for 1 hour, cooled and 2,3-dihydro-7-methoxy-4-oxo-4H-1-benzopyran, (77.9 g) in dry ether (440 ml) was added dropwise with stirring. After addition the reaction mixture was refluxed for 1 hour, cooled and the complex was decomposed by the addition of ammonium chloride solution. The ethereal layer was separated, washed with water and dried. Evaporation of the solvent left 76 g of the title compound as an oil (89%). MS and NMR analysis were correct for the required compound.

후처리

  1. customAfter the initial reaction
  2. temperaturewas refluxed for 1 hour
  3. temperaturecooled
  4. additionAfter addition the reaction mixture
  5. temperaturewas refluxed for 1 hour
  6. temperaturecooled
  7. customThe ethereal layer was separated
  8. washwashed with water
  9. customdried
  10. customEvaporation of the solvent
  11. waitleft 76 g of the title compound as an oil (89%)

출처 및 근거

ORD 기록
ord-04305d7c45334004821ab4e9eff0a8c9
출처 데이터셋
uspto-grants-1980_12
특허 번호
US04238606

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