反応式
C([CH:4]1[CH2:8][CH2:7][O:6][C:5]1=[O:9])(=O)C.[OH-].[Na+].[CH:12](=O)[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1>>[C:13]1([CH:12]2[C:8](=[CH2:4])[CH2:7][O:6][C:5]2=[O:9])[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1参加物
4
実験手順
The reaction was repeated using 3-acetyl-dihydro-2(3H)-furanone, sodium hydroxide and benzaldehyde to produce 3-phenyl methylene-dihydro-2(3H)-furanone. The crude yellow solid obtained from the reaction was recrystallized from chloroform to recover 3-phenylmethylene-dihydro-2(3H)-furanone, a yellow crystalline solid melting at 116° C. Proton and carbon nuclear magnetic resonance spectra for the product were as follows:
出典と根拠
- ORDレコード
- ord-8c59b05491e849e1b57e7f340ce9303a
- 出典データセット
- uspto-grants-1990_12
- 特許番号
- US04980342
関連ノート
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