反応式
[C:1]([O:7][CH2:8][CH:9]=[CH2:10])(=[O:6])[CH2:2][C:3]([CH3:5])=O.[NH:11]1[CH2:15][CH2:14][CH2:13][CH2:12]1>>[NH:11]1[CH2:15][CH2:14][CH2:13][CH:12]1[C:3]([CH3:5])=[CH:2][C:1]([O:7][CH2:8][CH:9]=[CH2:10])=[O:6]参加物
3
実験手順
Allyl 3-tetrahydropyrrolyl-2-butenoate was prepared (4.7 g, 68%) in the same manner as described in the above Example 1 (1) from allyl acetoacetate (5.0 g, 35.17 mmol) and pyrrolidine (8.8 mL, 105.51 mmol), and the obtained product was identified with the following 1H NMR data.
出典と根拠
- ORDレコード
- ord-b23c8ba54c484e1bafaf208e0e2e4633
- 出典データセット
- uspto-grants-2006_08
- 特許番号
- US07094908B2
関連ノート
読み込み中…