Pyridinium chloride → Ditriphenyleno[2,3-b:2',3'-d]thiophene-6,14-diol
反応式
C[O:2][C:3]1[CH:4]=[C:5]2[C:39](=[CH:40][CH:41]=1)[C:38]1[C:12](=[CH:13][C:14]3[C:18]4[CH:19]=[C:20]5[C:33](=[CH:34][C:17]=4[S:16][C:15]=3[CH:37]=1)[C:32]1[C:27](=[CH:28][C:29]([O:35]C)=[CH:30][CH:31]=1)[C:26]1[C:21]5=[CH:22][CH:23]=[CH:24][CH:25]=1)[C:11]1[C:6]2=[CH:7][CH:8]=[CH:9][CH:10]=1.Cl.N1C=CC=CC=1>>[CH:22]1[CH:23]=[CH:24][CH:25]=[C:26]2[C:21]=1[C:20]1[C:33]([C:32]3[C:27]2=[CH:28][C:29]([OH:35])=[CH:30][CH:31]=3)=[CH:34][C:17]2[S:16][C:15]3[CH:37]=[C:38]4[C:12]([C:11]5[C:6]([C:5]6[C:39]4=[CH:40][CH:41]=[C:3]([OH:2])[CH:4]=6)=[CH:7][CH:8]=[CH:9][CH:10]=5)=[CH:13][C:14]=3[C:18]=2[CH:19]=1参加物
3
反応条件
- 温度
- 220 °C
実験手順
A mixture of 9.8 g (18 mmol) of 6,14-dimethoxyditriphenyleno[2,3-b:2′,3′-d]thiophene, 31.2 g (270 mmol) of pyridine hydrochloride, was degassed and placed under nitrogen, and then heated at 220° C. for 6 h, the mixture was allowed to cool to room temperature and water was added. The resulting solid was filtered off, washed with water, and dried under high vacuum to give the product (8.2 g, 15.8 mmol, 88%).
後処理
- customwas degassed
- temperatureto cool to room temperature
- additionwater was added
- filtrationThe resulting solid was filtered off
- washwashed with water
- customdried under high vacuum
出典と根拠
- ORDレコード
- ord-5523ef82e52340db9051ec4d358d2672
- 出典データセット
- uspto-grants-2015_10
- 特許番号
- US09166177B2
反応ノート
読み込み中…