Ammonia → 6-chloro-3,4-dihydro-2-methyl-3-oxo-2H-1,4-benzoxazine-8-carboxylic acid

HRID 329710

反応式

HRID 329710 の反応式
[C:1]([C:4]1[CH:15]=[C:14]([Cl:16])[CH:13]=[C:12]([N+:17]([O-])=O)[C:5]=1[O:6][CH:7]([CH3:11])[C:8](O)=[O:9])([OH:3])=[O:2].N>O>[Cl:16][C:14]1[CH:15]=[C:4]([C:1]([OH:3])=[O:2])[C:5]2[O:6][CH:7]([CH3:11])[C:8](=[O:9])[NH:17][C:12]=2[CH:13]=1

参加物

4

反応物 2

HCID 222Ammonia2 回HCID 145172302-(2-Carboxy-4-chloro-6-nitrophenoxy)propionic acid

生成物 1

HCID 145172316-chloro-3,4-dihydro-2-methyl-3-oxo-2H-1,4-benzoxazine-8-carboxylic acid収率 92.2%

試薬・触媒・溶媒 1

HCID 962Water溶媒2 回

実験手順

To a solution of 960 g of ferrous sulfate heptahydrate in 2 1 of hot water is added a solution of 130 g of 2-(2-carboxy-4-chloro-6-nitrophenoxy)propionic acid and 200 ml of aqueous concentrated ammonia solution in 480 ml of water under stirring. After stirring for 30 minutes, to the reaction mixture is twice added 480 ml of aqueous concentrated ammonia solution. While the reaction mixture becomes exothermic, stirring is continued for an hour. The resultant mixture is filtered through a celite layer under reduced pressure and washed with 2 1 of hot water twice. The filtrate is cooled and made acid with concentrated hydrochloric acid. The precipitated crystals are washed with water and dried to give 100 g of 6-chloro-3,4-dihydro-2 -methyl-3-oxo-2H-1,4-benzoxazine-8-carboxylic acid, melting at 319°-320° C. with decomposition.

後処理

  1. stirringAfter stirring for 30 minutes, to the reaction mixture
  2. stirringstirring
  3. waitis continued for an hour
  4. filtrationThe resultant mixture is filtered through a celite layer under reduced pressure
  5. washwashed with 2 1 of hot water twice
  6. temperatureThe filtrate is cooled
  7. washThe precipitated crystals are washed with water
  8. customdried

出典と根拠

ORDレコード
ord-d0cff010fc964bb5993de023b74ae6f4
出典データセット
uspto-grants-1990_01
特許番号
US04892872

関連ノート

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