p-Toluenesulfonic acid → 2-(4-Fluorophenyl)benzoxazole
反応式
C1(C)C=CC(S(O)(=O)=O)=CC=1.[F:12][C:13]1[CH:28]=[CH:27][C:16]([C:17]([NH:19][C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][C:21]=2[OH:26])=O)=[CH:15][CH:14]=1>>[F:12][C:13]1[CH:28]=[CH:27][C:16]([C:17]2[O:26][C:21]3[CH:22]=[CH:23][CH:24]=[CH:25][C:20]=3[N:19]=2)=[CH:15][CH:14]=1参加物
3
反応条件
- 温度
- 110 °C
実験手順
After the flask containing 4-Fluoro-N-(2-hydroxyphenyl)-benzamide in 250 ml of toluene of step 1 was equipped with a Dean-Stark apparatus, p-toluenesulfonic acid (12.2 g, 64 mmol, 0.2 eq) was added. The mixture was stirred at 110° C. for 8 hours. Then heating was stopped and the solution was subsequently washed with 100 ml of water, 2*100 ml of (0.2M) NaOH solution and 100 ml of water. Toluene was removed via rotary evaporator yielding 64 g (94%) of slightly off white 2-(4-fluorophenyl)-1,3-benzoxazole.
後処理
- additionwas added
- temperatureThen heating
- washthe solution was subsequently washed with 100 ml of water, 2*100 ml of (0.2M) NaOH solution and 100 ml of water
- customToluene was removed via rotary evaporator
出典と根拠
- ORDレコード
- ord-f89ceeca103e4eb7964c7864d86eeaec
- 出典データセット
- uspto-grants-2016_09
- 特許番号
- US09440935B2
反応ノート
読み込み中…