Potassium Hydroxide → HCID 13145802、化合物

HRID 1074545ノート

反応式

HRID 1074545 の反応式
[OH-].[K+].[F:3][C:4]1[CH:5]=[C:6]([CH:16]=[CH:17][CH:18]=1)[CH2:7][O:8][C:9]1[CH:14]=[CH:13][C:12]([OH:15])=[CH:11][CH:10]=1.Cl[CH2:20][CH2:21][CH2:22][N:23]1[CH2:28][CH2:27][O:26][CH2:25][CH2:24]1>C(O)C>[F:3][C:4]1[CH:5]=[C:6]([CH:16]=[CH:17][CH:18]=1)[CH2:7][O:8][C:9]1[CH:14]=[CH:13][C:12]([O:15][CH2:20][CH2:21][CH2:22][N:23]2[CH2:28][CH2:27][O:26][CH2:25][CH2:24]2)=[CH:11][CH:10]=1

参加物

5

実験手順

To a solution of 0.56 g (0.01 mol) of potassium hydroxide in 18 ml of absolute ethanol are added 2.18 g (0.01 mol) of 4-(3-fluorobenzyloxy)phenol. There is then added a solution of 1.64 g (0.01 mol) of N-(3-chloropropyl)morpholine in 2 ml of absolute ethanol. The mixture is stirred at reflux for 24 hours, allowed to cool and then refrigerated. The solid which forms is collected by filtration, washed with absolute ethanol and dissolved in diethyl ether. The ethereal solution is washed consecutively with water (20 ml), 10% aqueous sodium hydroxide (3×15 ml) and water until neutral to litmus. The solution is dried over sodium sulfate, filtered and evaporated and recrystallized from diethyl ether-petroleum ether and from diethyl ether alone to yield N-[3-(4-{3-fluorobenzyloxy}phenoxy)propyl]morpholine.

後処理

  1. temperatureat reflux for 24 hours
  2. temperatureto cool
  3. filtrationThe solid which forms is collected by filtration
  4. washwashed with absolute ethanol
  5. dissolutiondissolved in diethyl ether
  6. washThe ethereal solution is washed consecutively with water (20 ml), 10% aqueous sodium hydroxide (3×15 ml) and water until neutral to litmus
  7. dry with materialThe solution is dried over sodium sulfate
  8. filtrationfiltered
  9. customevaporated
  10. customrecrystallized from diethyl ether-petroleum ether and from diethyl ether alone

出典と根拠

ORDレコード
ord-c72717f097ab4d5d86c01c5367f111de
出典データセット
uspto-grants-1983_07
特許番号
US04393061

反応ノート

読み込み中…