Iodoethane → HCID 22845729、化合物
反応式
Cl.[CH2:2]([O:4][C:5]([C@@H:7]1[CH2:11][C@H:10]([OH:12])[CH2:9][NH:8]1)=[O:6])[CH3:3].[CH2:13](N(CC)CC)[CH3:14].C(I)C>C(Cl)(Cl)Cl>[CH2:2]([O:4][C:5]([C@@H:7]1[CH2:11][C@H:10]([OH:12])[CH2:9][N:8]1[CH2:13][CH3:14])=[O:6])[CH3:3]参加物
5
実験手順
To a suspension of 12 g of (2S,4S)-2-ethoxycarbonyl-4-hydroxy pyrrolidine hydrochloride obtained in the preceeding para. (1) in 60 ml of chloroform, were added 12.42 g of triethylamine and the combined was added with 17.22 g of ethyl iodide and heat-refluxed for 4 hours. The reaction mixture was after-treated to obtain (2S,4S)2-ethoxycarbonyl-N-ethyl-4-hydroxy pyrrolidine as an oily (product Yield 9.55 g.
後処理
- customobtained in the preceeding para
- temperatureheat-refluxed for 4 hours
- additionThe reaction mixture was after-treated
出典と根拠
- ORDレコード
- ord-69f847d9b4b64331bc51cefcaf71c876
- 出典データセット
- uspto-grants-1992_09
- 特許番号
- US05143935
反応ノート
読み込み中…