Water → 1-(Benzoyloxy)-2-methyl-2-propanaminium chloride

HRID 1764323ノート

反応式

HRID 1764323 の反応式
[ClH:1].[C:2]1([C:8]2[O:9][CH2:10][C:11]([CH3:14])([CH3:13])[N:12]=2)[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[OH2:15]>Cl.O1CCCC1>[ClH:1].[C:8]([O:9][CH2:10][C:11]([NH2:12])([CH3:14])[CH3:13])(=[O:15])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

参加物

5

反応物 2

HCID 962WaterHCID 12220134Oxazole, 4,5-dihydro-4,4-dimethyl-2-phenyl-, hydrochloride

生成物 1

HCID 546091031-(Benzoyloxy)-2-methyl-2-propanaminium chloride

試薬・触媒・溶媒 2

HCID 313Hydrochloric Acid溶媒HCID 8028Tetrahydrofuran溶媒

実験手順

To 8.7 g (0.041 mol) 2-phenyl-4,4-dimethyl-1,3-oxazoline hydrochloride suspended in 120 ml anhydrous hydrogen chloride in tetrahydrofuran (1M) was added 3.6 ml (0.20 mol) water. The mixture was warmed to cause solution and heated under reflux with stirring for 1 hour. The tetrahydrofuran was removed under reduced pressure to afford a nearly colorless oil which crystallized at 0° following the addition of anhydrous ether. The solid was triturated with anhydrous ether overnight and isolated by filtration under a nitrogen atmosphere. After drying in vacuo over calcium sulfate, 6.9 g (0.30 mol), 73%, 2-amino-2-methyl-1-propyl benzoate hydrochloride was obtained as a white solid, mp 225°-228° (dec.) acetone:hexane, ir (KBr) 1725 (c=o) cm-1, pmr (D2O) δ 1.50 (s, 6H), 4.4 (s, 2H) and 7.0 - 8.3 (m, 5H) ppm.

後処理

  1. temperatureThe mixture was warmed
  2. temperatureheated
  3. temperatureunder reflux
  4. customThe tetrahydrofuran was removed under reduced pressure
  5. customto afford a nearly colorless oil which
  6. customcrystallized at 0°
  7. additionthe addition of anhydrous ether
  8. customThe solid was triturated with anhydrous ether overnight
  9. customisolated by filtration under a nitrogen atmosphere
  10. dry with materialAfter drying in vacuo over calcium sulfate, 6.9 g (0.30 mol), 73%

出典と根拠

ORDレコード
ord-e919bfa746e1442fa0974ddc17325e9a
出典データセット
uspto-grants-1978_09
特許番号
US04115588

反応ノート

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