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

HRID 1386031
ノート
印刷プレビュー

反応式

HRID 1386031 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

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

生成物 1

HCID 109113966-Bromo-4-methoxy-1,3-dioxaindane収率 52%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-225f8935131a42c6a2c36c5d1dbedf44
出典データセット
uspto-grants-2001_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06265399B1

反応ノート

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