反応式
[OH:1][C:2]1[CH:3]=[C:4]([CH:7]=[C:8]([C:11]#[N:12])[C:9]=1[OH:10])[CH:5]=O.[CH3:13][CH2:14][C:15](=[O:19])[CH2:16][CH:17]=[O:18].N1CCCCC1.C(O)(=O)C>C1(C)C=CC=CC=1>[OH:1][C:2]1[CH:3]=[C:4]([CH:5]=[C:16]([CH:17]=[O:18])[C:15](=[O:19])[CH2:14][CH3:13])[CH:7]=[C:8]([C:11]#[N:12])[C:9]=1[OH:10]参加物
6
実験手順
A mixture 1.6 g of 3,4-dihydroxy-5-cyanobenzaldehyde, 2.0 g of 3,5-pentanedione, 0.2 ml of piperidine and 0.6 ml of acetic acid in 70 ml of toluene was refluxed for 2 h with Dean-Stark separator. The solvent was evaporated in vacuo and the residue was crystallized from acetone-cyclohexane. mp 228°-232° C.
後処理
- customThe solvent was evaporated in vacuo
- customthe residue was crystallized from acetone-cyclohexane
出典と根拠
- ORDレコード
- ord-dd5989d39665475cb846a8388674bb9e
- 出典データセット
- uspto-grants-1996_02
- 特許番号
- US05489614
関連ノート
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