反応式
[OH:1][C:2]1[CH:12]=[CH:11][C:5]([CH:6]=[CH:7]C(O)=O)=[CH:4][CH:3]=1.C1(C=CC(O)=CC=1)O.N12CCCN=C1CCCCC2>CS(C)=O>[OH:1][C:2]1[CH:12]=[CH:11][C:5]([CH:6]=[CH2:7])=[CH:4][CH:3]=1参加物
5
反応条件
- 温度
- 135 °C
実験手順
In a 1-liter sulfonating flask equipped with mechanical stirrer, reflux condenser and nitrogen delivery line, 300 ml of dimethyl sulfoxide are added to 150 g (0.91 mol) of 4-hydroxycinnamic acid, 6 g (54 mmol) of hydroquinone and 6 g (39 mmol) of 1,8-diazabicyclo[5.4.0]undec-7-ene. The mixture is then heated at 135° C. for 31/2 hours. After cooling, the mixture is poured onto ice and extracted three times with 500 ml of diethyl ether, and the organic phase is washed five times with 100 ml of water, dried over magnesium sulfate and concentrated. The resulting oil is recrystallised twice from n-hexane to yield 69.07 g (0.58 mol, 63% of the theoretical yield) of 4-hydroxystyrene in the form of a white powder (m.p. 68° C.).
後処理
- customequipped with mechanical stirrer
- temperaturereflux condenser
- temperatureAfter cooling
- additionthe mixture is poured onto ice
- extractionextracted three times with 500 ml of diethyl ether
- washthe organic phase is washed five times with 100 ml of water
- dry with materialdried over magnesium sulfate
- concentrationconcentrated
- customThe resulting oil is recrystallised twice from n-hexane
- customto yield 69.07 g (0.58 mol, 63% of the
出典と根拠
- ORDレコード
- ord-dee086b3dbe7405ca4cdb115ec555481
- 出典データセット
- uspto-grants-1993_12
- 特許番号
- US05274060
関連ノート
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