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Dibromomethane → 6-Bromo-4-methoxy-1,3-dioxaindane

HRID 1069487
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HRID 1069487 반응식
[Br:1][C:2]1[CH:7]=[C:6]([O:8][CH3:9])[C:5]([OH:10])=[C:4]([OH:11])[CH:3]=1.[C:12](=O)([O-])[O-].[K+].[K+].BrCBr>CN(C)C=O>[Br:1][C:2]1[CH:3]=[C:4]([O:11][CH3:12])[C:5]2[O:10][CH2:9][O:8][C:6]=2[CH:7]=1
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참가 물질

5

반응물 3

HCID 3024DibromomethaneHCID 11430Potassium CarbonateHCID 109877565-Bromo-3-methoxybenzene-1,2-diol

생성물 1

HCID 109113966-Bromo-4-methoxy-1,3-dioxaindane수율 52%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

To dimethylformamide (400 mL) was added 1-bromo-3,4-dihydroxy-5-methoxybenzene (40 g, 182 mmol), potassium carbonate (75.7 g, 548 mmol), and dibromomethane (95.2 g, 548 mmol), followed by heating to reflux for 1 hour. The solvent was evaporated in vacuo, and the residue was taken up into ethyl ether, filtered, washed with saturated potassium carbonate solution, brine, 1N citric acid solution, and brine. The organic phase was dried over anhydrous magnesium sulfate and filtered through charcoal. The filtrate was concentrated in vacuo giving a crystalline precipitate which was filtered, washed with hexane, and dried in vacuo to a solid. This material was distilled at 2 mm Hg, 125° C., giving a crystalline solid, 21.7 g, 52% yield. NMR spectra and elemental analysis were consistent with the structure.

후처리

  1. temperatureby heating
  2. temperatureto reflux for 1 hour
  3. customThe solvent was evaporated in vacuo
  4. filtrationfiltered
  5. washwashed with saturated potassium carbonate solution, brine, 1N citric acid solution, and brine
  6. dry with materialThe organic phase was dried over anhydrous magnesium sulfate
  7. filtrationfiltered through charcoal
  8. concentrationThe filtrate was concentrated in vacuo
  9. customgiving a crystalline precipitate which
  10. filtrationwas filtered
  11. washwashed with hexane
  12. customdried in vacuo to a solid
  13. distillationThis material was distilled at 2 mm Hg, 125° C.
  14. customgiving a crystalline solid, 21.7 g, 52% yield

출처 및 근거

ORD 기록
ord-33add3b8bb9444f4bc4bd705b53c3c86
출처 데이터셋
uspto-grants-2001_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06252070B1

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