反応式
[C:1]([OH:6])(=[O:5])[C:2]([CH3:4])=[CH2:3].[O:7]1[CH:12]=[CH:11][CH2:10][CH2:9][CH2:8]1.Cl.C(=O)(O)[O-].[Na+]>[N+](C1C=C([N+]([O-])=O)C=CC=1C)([O-])=O.Cl>[C:1]([O:6][CH:8]1[CH2:9][CH2:10][CH2:11][CH2:12][O:7]1)(=[O:5])[C:2]([CH3:4])=[CH2:3]参加物
7
反応条件
- 温度
- 50 °C
実験手順
to a solution of 25.8 g (0.3 mol) methacrylic acid and 1.8 g (0.011 mol) 2,4-dinitrotoluene in 25.2 g (0.3 mol) dihydropyran was added 0.05 ml (0.0015 mol) concentrated hydrochloric acid. The reaction mixture was allowed to stir at 50° C. for 25 hr. The hydrochloric acid was neutralized with solid sodium bicarbonate and the mixture was filtered. The filtrate was distilled to give 46.5 g (0.273 mol, 91% yield) tetrahydropyran-2-yl methacrylate, bp 50° C. at 0.15 torr.
後処理
- filtrationthe mixture was filtered
- distillationThe filtrate was distilled
出典と根拠
- ORDレコード
- ord-a4b22e8e27be4e7fb3eadcb1543bfa82
- 出典データセット
- uspto-grants-1993_07
- 特許番号
- US05225316
関連ノート
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