Water → 2-Chloro-6-nitro-3-pyrrolidinobenzonitrile
反応式
[Cl:1][C:2]1[C:9](Cl)=[CH:8][CH:7]=[C:6]([N+:11]([O-:13])=[O:12])[C:3]=1[C:4]#[N:5].[NH:14]1[CH2:18][CH2:17][CH2:16][CH2:15]1.O>CN(C)C=O>[Cl:1][C:2]1[C:9]([N:14]2[CH2:18][CH2:17][CH2:16][CH2:15]2)=[CH:8][CH:7]=[C:6]([N+:11]([O-:13])=[O:12])[C:3]=1[C:4]#[N:5]参加物
5
実験手順
13.0 g of 2,3-dichloro-6-nitrobenzonitrile was dissolved in 50 ml of dimethylformamide, and 11.0 g of pyrrolidine was added to the solution, followed by stirring while externally cooling because of heat generation. After continuing the stirring for 30 minutes, the reaction mixture was poured into water. The precipitate thus formed was filtered, washed with water and then with methanol to obtain 13.3 g of 2-chloro-6-nitro-3-pyrrolidinobenzonitrile (melting point: 170°-173° C.).
後処理
- temperaturewhile externally cooling because of heat generation
- customstirring for 30 minutes
- customThe precipitate thus formed
- filtrationwas filtered
- washwashed with water
出典と根拠
- ORDレコード
- ord-25bd0f96e9344708b7d10565fea58a47
- 出典データセット
- uspto-grants-1986_09
- 特許番号
- US04610987
反応ノート
読み込み中…