Acetone → 7-Methoxymethoxy-3-(4-methoxymethoxyphenyl)-3-methylthiochroman-4-one

HRID 1859339ノート

反応式

HRID 1859339 の反応式
C[C:2](C)=[O:3].[OH:5][C:6]1[CH:15]=[C:14]2[C:9]([C:10](=[O:24])[C:11]([C:17]3[CH:22]=[CH:21][C:20]([OH:23])=[CH:19][CH:18]=3)([CH3:16])[CH2:12][S:13]2)=[CH:8][CH:7]=1.[C:25](=O)([O-])[O-].[K+].[K+].[CH3:31][O:32][CH2:33]Cl>O>[CH3:31][O:32][CH2:33][O:5][C:6]1[CH:15]=[C:14]2[C:9]([C:10](=[O:24])[C:11]([C:17]3[CH:22]=[CH:21][C:20]([O:23][CH2:25][O:3][CH3:2])=[CH:19][CH:18]=3)([CH3:16])[CH2:12][S:13]2)=[CH:8][CH:7]=1

参加物

6

実験手順

To dry acetone solution (100 ml) of 7-hydroxy-3-(4-hydroxyphenyl)-3-methylthiochroman-4-one (2.30 g, 8.04 mmol) were added potassium carbonate (8.87 g, 64.3 mmol) and methoxymethyl chloride (4.64 ml, 61.5 mmol), and the mixture was heated under refluxing for 40 hours. After adding water, the reaction solution was extracted with ethyl acetate. The organic layer was washed with saturated saline, dried over anhydrous magnesium sulfate and then distilled under reduced pressure to remove the solvent. The crude product thus obtained was purified with silica gel column chromatography (ethyl acetate:hexane=1:3) to obtain 2.65 g (yield: 88%) of the title compound.

後処理

  1. temperaturethe mixture was heated
  2. temperatureunder refluxing for 40 hours
  3. extractionthe reaction solution was extracted with ethyl acetate
  4. washThe organic layer was washed with saturated saline
  5. dry with materialdried over anhydrous magnesium sulfate
  6. distillationdistilled under reduced pressure
  7. customto remove the solvent
  8. customThe crude product thus obtained
  9. customwas purified with silica gel column chromatography (ethyl acetate:hexane=1:3)

出典と根拠

ORDレコード
ord-63e273ff366f476faa546b9ffcda0c6a
出典データセット
uspto-grants-2000_11
特許番号
US06153768

反応ノート

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