反応式
[I:1][C:2]1[CH:9]=[C:8]([Cl:10])[CH:7]=[C:4]([CH:5]=O)[C:3]=1[OH:11].[C:12](OC(=O)C)(=[O:14])[CH3:13]>C(N(CC)CC)C>[Cl:10][C:8]1[CH:7]=[C:4]2[C:3](=[C:2]([I:1])[CH:9]=1)[O:11][C:12](=[O:14])[CH:13]=[CH:5]2参加物
4
実験手順
A mixture of 3-iodo-5-chlorosalicylaldehyde (100 g, 0.354 mole), acetic anhydride (300 mL) and triethylamine (54 mL) was heated at reflux for 18 hours. Upon cooling, the desired coumarin precipitated as a dark brown crystalline material. This was filtered, washed with hexane/ethyl acetate (4:1, 200 mL), and was air dried. Yield: 60 g (55%).
後処理
- temperaturewas heated
- temperatureat reflux for 18 hours
- temperatureUpon cooling
- customthe desired coumarin precipitated as a dark brown crystalline material
- filtrationThis was filtered
- washwashed with hexane/ethyl acetate (4:1, 200 mL)
- customdried
出典と根拠
- ORDレコード
- ord-ab41251c244b49318e2bfc4e760e2a8c
- 出典データセット
- uspto-grants-2002_04
- 特許番号
- US06372719B1
関連ノート
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