Acetic Acid → 2-Chloro-5-ethylpyridine
反応式
[N:1]1([CH:6]=[CH:7][C:8]#N)[CH2:5][CH2:4][CH2:3][CH2:2]1.N1(C=CCC)CCCC1.C(O)(=O)C.[ClH:23]>C(Cl)(Cl)Cl>[Cl:23][C:6]1[CH:7]=[CH:8][C:4]([CH2:3][CH3:2])=[CH:5][N:1]=1参加物
6
実験手順
19.3 g of β-pyrrolidino-acrylonitrile were added at -10° C. to 30 g of pyrrolidino-butene from A4 in 50 ml of chloroform. The mixture was allowed to warmto RT, and 50 ml of acetic acid were added dropwise. After stirring at RT for 15 hours, the mixture was cooled to -10° C., and dry hydrogen chloride gas was introduced. Aqueous workup gave 2-chloro-5-ethylpyridine as the main product.
後処理
- customto warmto RT
- temperaturethe mixture was cooled to -10° C.
出典と根拠
- ORDレコード
- ord-14b569afbedf4364a9df29d744aacb65
- 出典データセット
- uspto-grants-1995_11
- 特許番号
- US05466800
反応ノート
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