反応式
CC1C=C2[C:8](=[CH:9][CH:10]=1)N[C:6](=[O:11])C2.[CH3:12][C:13]([O-:15])=O.[Na+].[C:17](O)(=O)C>>[CH3:6][OH:11].[O:15]([CH:9]([CH3:8])[CH3:10])[CH:13]([CH3:12])[CH3:17]参加物
4
実験手順
A mixture of 5-methyl-2-oxindole (2.94 g, 0.02 mol), 3,5-di-tertiary-butyl-4-hydroxybenzoldehyde (4.68 g, 0.02 mol), and anyydrous NaOAc (5.75 g, 0.07 mol) in glacial acetic acid (100 mL) was heated to reflux for 18 hours. The cooled reaction mixture was poured into ice-water mixture when a yellow product precipitated out. It was recrystallized from CH2Cl2 --CH3OH-iso-Pr2O to give the analytical sample. Yield 2.16 g (28.7%), mp 230°-234° C.
後処理
- temperaturewas heated
- temperatureto reflux for 18 hours
- customThe cooled reaction mixture
- customprecipitated out
- customIt was recrystallized from CH2Cl2
出典と根拠
- ORDレコード
- ord-9e9feb137dcb4903abe56920c948ff41
- 出典データセット
- uspto-grants-1992_06
- 特許番号
- US05124347
関連ノート
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