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Sodium Hydroxide → 2-p-Chlorophenyl-5-(2,5-dimethylphenoxy)-4-oxazoleacetic acid

HRID 46768
ノート
印刷プレビュー

反応式

HRID 46768 の反応式
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[O:9][C:10]([O:18][C:19]3[CH:24]=[C:23]([CH3:25])[CH:22]=[CH:21][C:20]=3[CH3:26])=[C:11]([CH2:13][C:14]([O:16]C)=[O:15])[N:12]=2)=[CH:4][CH:3]=1.[OH-].[Na+]>CC(C)=O>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[O:9][C:10]([O:18][C:19]3[CH:24]=[C:23]([CH3:25])[CH:22]=[CH:21][C:20]=3[CH3:26])=[C:11]([CH2:13][C:14]([OH:16])=[O:15])[N:12]=2)=[CH:4][CH:3]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 14798Sodium HydroxideHCID 20385655HCID 20385655、化合物

生成物 1

HCID 203856742-p-Chlorophenyl-5-(2,5-dimethylphenoxy)-4-oxazoleacetic acid収率 72.3%

試薬・触媒・溶媒 1

HCID 180Acetone溶媒

実験手順

To a stirred solution of 13 g of methyl 2-p-chlorophenyl-5-(2,5-dimethylphenoxy)-4-oxazoleacetate prepared in Example 4 in 150 ml of acetone at room temperature was dropwise added a 15 ml aqueous solution of 2.0 g of sodium hydroxide. The mixture was further stirred for 3.5 hours. After the solvent was evaporated under reduced pressure, water was added to the remaining aqueous solution. The resulting solution was cooled and acidified to pH 3 with hydrochloric acid. The crystalline precipitate was filtered off and recrystallized from ethanol to give 9.05 g of the title compound as bulky needles, melting at 185° C.

後処理

  1. customAfter the solvent was evaporated under reduced pressure, water
  2. additionwas added to the remaining aqueous solution
  3. temperatureThe resulting solution was cooled
  4. filtrationThe crystalline precipitate was filtered off
  5. customrecrystallized from ethanol

出典と根拠

ORDレコード
ord-2f261490df9f4084ba563ae7f2b4df4d
出典データセット
uspto-grants-1979_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04175130

反応ノート

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