Butanal → 1-But-1-enylpyrrolidine
反応式
[CH:1](=O)[CH2:2][CH2:3][CH3:4].[NH:6]1[CH2:10][CH2:9][CH2:8][CH2:7]1.C(=O)([O-])[O-].[K+].[K+]>C1(C)C=CC=CC=1>[N:6]1([CH:7]=[CH:8][CH2:9][CH3:10])[CH2:4][CH2:3][CH2:2][CH2:1]1参加物
5
実験手順
108 g of freshly distilled butyraldehyde were added dropwise at 0° C. to a mixture of 213 g of pyrrolidine and 213 g of potassium carbonate. The mixture was allowed to stand overnight at room temperature, diluted with 300 ml of toluene, and the residue was filtered off. The filtrate was then subjected to vacuum distillation at 85° to 90° C. (80 mbar), giving 102 g of 97% pure 1-pyrrolidinobutene, which corresponds to 63.7% of the theoretical yield).
後処理
- filtrationthe residue was filtered off
- distillationThe filtrate was then subjected to vacuum distillation at 85° to 90° C. (80 mbar)
出典と根拠
- ORDレコード
- ord-d3697e5b00e64347a24e9c7a729501b3
- 出典データセット
- uspto-grants-1995_11
- 特許番号
- US05466800
反応ノート
読み込み中…