反応式
[C:1]([OH:11])(=O)/[CH:2]=[CH:3]/[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.C(Cl)(=O)C([Cl:15])=O>C1(C)C=CC=CC=1>[C:1]([Cl:15])(=[O:11])/[CH:2]=[CH:3]/[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1参加物
4
反応条件
- 温度
- 0 °C
実験手順
trans-Cinnamic acid (5 g, 33.7 mmol, Aldrich) was dissolved in toluene (100 mL), and the solution was cooled to 0° C. and flushed with N2. Anhydrous DMF (0.1 mL) was added, followed by oxalyl chloride (8.56 g, 5.88 mL, 67.4 mmol) dropwise over 8 minutes. The mixture was stirred at 0° C. for 1 hour and at room temperature for 1.5 hours. The solvent was removed under vacuum to give the title compound (7.63 g).
後処理
- customflushed with N2
- additionAnhydrous DMF (0.1 mL) was added
- customThe solvent was removed under vacuum
出典と根拠
- ORDレコード
- ord-5922897b2fd84ef282b4a00b663a2f4c
- 出典データセット
- uspto-grants-1997_04
- 特許番号
- US05618949
関連ノート
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