反応式
[OH:1][C:2]1[CH:3]=[C:4]([C:9](=[O:11])[CH3:10])[CH:5]=[C:6]([OH:8])[CH:7]=1.[CH3:12]I.[H-].[Na+]>CN(C=O)C.CC(=O)OCC>[OH:1][C:2]1[CH:3]=[C:4]([C:9](=[O:11])[CH3:10])[CH:5]=[C:6]([O:8][CH3:12])[CH:7]=1参加物
6
実験手順
1-(3,5-Dihydroxyphenyl)ethanone (3 g) and methyl iodide (2.80 g) were dissolved in DMF (40 ml), and sodium hydride (568 mg) was added. After stirring at RT for 2 h, the DMF was drawn off. The residue was taken up in EA and washed with water, dried, filtered and concentrated. The residue was purified using silica gel (89 g cartridge, n-heptane/EA 0-50% within 30 min). 1.12 g of the title compound were obtained.
後処理
- washwashed with water
- customdried
- filtrationfiltered
- concentrationconcentrated
- customThe residue was purified
- customsilica gel (89 g cartridge, n-heptane/EA 0-50% within 30 min)
出典と根拠
- ORDレコード
- ord-f95df772e1fa45d7b30c9cdf1ff92fb1
- 出典データセット
- uspto-grants-2012_06
- 特許番号
- US08198272B2
関連ノート
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