反応式
[CH3:1][C:2]([C:4]([CH3:6])=[CH2:5])=[CH2:3].[CH3:7][O:8][C:9](=[O:16])[C:10]#[C:11][C:12]([O:14][CH3:15])=[O:13]>C1C=CC=CC=1>[CH3:7][O:8][C:9]([C:10]1[CH2:5][C:4]([CH3:6])=[C:2]([CH3:3])[CH2:1][C:11]=1[C:12]([O:14][CH3:15])=[O:13])=[O:16]参加物
4
実験手順
2,3-Dimethyl-buta-1,3-diene (2.0 g, 24.3 mmol) and but-2-ynedioic acid dimethyl ester in benzene (14 mL) were heated to reflux for 16 h. The resulting mixture was cooled and evaporated in vacuo to yield a solid, which was purified via flash column chromatography (EtOAc/heptane 9:1) to yield 4,5-dimethyl-cyclohexa-1,4-diene-1,2-dicarboxylic acid dimethyl ester as a white solid.
後処理
- temperatureto reflux for 16 h
- temperatureThe resulting mixture was cooled
- customevaporated in vacuo
- customto yield a solid, which
- customwas purified via flash column chromatography (EtOAc/heptane 9:1)
出典と根拠
- ORDレコード
- ord-4307b53bc2a749249ff6a351f85daebc
- 出典データセット
- uspto-grants-2014_03
- 特許番号
- US08673890B2
関連ノート
読み込み中…