Hydrogen Bromide → 2,6-Diphenylpyridine hydrobromide
反応式
[BrH:1].[C:2]1([C:8]2[CH:13]=[CH:12][CH:11]=[C:10]([C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=3)[N:9]=2)[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1>C1(C)C=CC=CC=1>[BrH:1].[C:14]1([C:10]2[CH:11]=[CH:12][CH:13]=[C:8]([C:2]3[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=3)[N:9]=2)[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=1参加物
4
実験手順
Hydrogen bromide gas is introduced into a solution of 30 g (0.130 mole) of 2,6-diphenylpyridine in 150 ml of toluene. The solid which forms is isolated by vacuum filtration. The filtrate is retreated with hydrogen bromide until no more solid is formed. The solid is then dried in vacuo. The product has a melting point of 161° C.-162° C.
後処理
- customThe solid which forms is isolated by vacuum filtration
- customis formed
- customThe solid is then dried in vacuo
出典と根拠
- ORDレコード
- ord-60faa63473cd46718136fe30ba636c9d
- 出典データセット
- uspto-grants-1987_02
- 特許番号
- US04640831
反応ノート
読み込み中…