反応式
[CH3:1][Si:2]([CH3:11])([CH3:10])[O:3][C:4]1[CH:9]=CC[CH2:6][CH:5]=1.[C:12]([O:17][CH3:18])(=[O:16])[C:13]#[C:14][CH3:15]>C1(C)C=CC=CC=1>[CH3:15][C:14]1[CH:9]=[C:4]([O:3][Si:2]([CH3:11])([CH3:10])[CH3:1])[CH:5]=[CH:6][C:13]=1[C:12]([O:17][CH3:18])=[O:16]参加物
4
反応条件
- 温度
- 150 °C
実験手順
A 50 mL round bottom flask equipped with magnetic stir bar and condenser was charged with 6.0 g of 2-trimethylsilyloxy-1,3-cyclohexadiene, 3.5 g methyl tetrolate in 3 mL dry toluene. The reaction was heated to 150° C. for 50 hours at which point 1H-NMR indicated no starting diene. The raction was concentrated in vacuo to provide 5.7 g (67%) methyl 2-methyl-4-trimethylsilyloxybenzoate.
後処理
- customA 50 mL round bottom flask equipped with magnetic stir bar and condenser
- concentrationThe raction was concentrated in vacuo
出典と根拠
- ORDレコード
- ord-940abf4bfb13441ca0e82923ec97ca9d
- 出典データセット
- uspto-grants-2006_11
- 特許番号
- US07141609B2
関連ノート
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