2(3H)-Benzoxazolone → 6-(3-Chloropropanoyl)-1,3-benzoxazol-2(3H)-one

HRID 654433ノート

反応式

HRID 654433 の反応式
[Cl-].[Al+3].[Cl-].[Cl-].[CH:5]1[CH:6]=[CH:7][C:8]2[O:14][C:12](=[O:13])[NH:11][C:9]=2[CH:10]=1.[Cl:15][CH2:16][CH2:17][C:18](Cl)=[O:19]>CN(C)C=O>[Cl:15][CH2:16][CH2:17][C:18]([C:6]1[CH:5]=[CH:10][C:9]2[NH:11][C:12](=[O:13])[O:14][C:8]=2[CH:7]=1)=[O:19]

参加物

5

反応物 3

HCID 60432(3H)-BenzoxazoloneHCID 693643-Chloropropionyl chlorideHCID 6451240Aluminum(III) Chloride

生成物 1

HCID 117908766-(3-Chloropropanoyl)-1,3-benzoxazol-2(3H)-one

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

56.1 g (0.42 mole) of aluminum chloride are weighed into a ground-necked flask, 10 cm3 of dimethylformamide are then added using a dropping funnel and the mixture is left stirring until it becomes homogeneous. 8.1 g (0.06 mole) of benzoxazolinone are then added and the mixture is left stirring for 10 minutes before adding 7 cm3 (0.072 mole) of 3-chloropropionic acid chloride. This mixture is maintained in an oil bath at 80°-85° C. for approximately 2 hours 30 minutes. After cooling, the reaction mixture is poured into ice-cold water. The precipitate is drained and washed with water to neutrality. The product is recrystallized in ethanol.

後処理

  1. waitthe mixture is left
  2. waitthe mixture is left
  3. stirringstirring for 10 minutes
  4. temperatureThis mixture is maintained in an oil bath at 80°-85° C. for approximately 2 hours 30 minutes
  5. temperatureAfter cooling
  6. additionthe reaction mixture is poured into ice-cold water
  7. washwashed with water to neutrality
  8. customThe product is recrystallized in ethanol

出典と根拠

ORDレコード
ord-115e79cdb56f45cb9e47650fe4e039df
出典データセット
uspto-grants-1992_07
特許番号
US05132305

反応ノート

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