Ethanol → 3-Phenyl-2,1-benzisoxazole-5-acetic acid

HRID 1199017ノート

反応式

HRID 1199017 の反応式
[C:1]1([C:7]2[O:8][N:9]=[C:10]3[CH:15]=[CH:14][C:13]([CH2:16][C:17]#N)=[CH:12][C:11]=23)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.C(O)C.[OH-:22].[Na+].[OH2:24]>>[C:1]1([C:7]2[O:8][N:9]=[C:10]3[CH:15]=[CH:14][C:13]([CH2:16][C:17]([OH:24])=[O:22])=[CH:12][C:11]=23)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1

参加物

5

反応物 4

HCID 702EthanolHCID 962WaterHCID 14798Sodium HydroxideHCID 148353463-Phenyl-2,1-benzisoxazole-5-acetonitrile

生成物 1

HCID 148353913-Phenyl-2,1-benzisoxazole-5-acetic acid収率 54%

実験手順

A solution of 5.0 g (0.021 mole) of 3-phenyl-2,1-benzisoxazole-5-acetonitrile, 100 ml of ethanol, and 10 ml of 20% sodium hydroxide was heated at reflux under a nitrogen atmosphere for 20 hr. The solution was poured into 800 ml of water, let stand for 0.5 hr and filtered. The filtrate was treated with charcoal, filtered, and the filtrate made acidic with concentrated hydrochloric acid. The mixture was allowed to stand at ambient temperature overnight and then filtered. The filter cake was washed with water, air dried, and recrystallized from 2-propanol to yield 2.9 g (54%) of gray powder, m.p. 173°-174° C. with decomposition.

後処理

  1. temperatureat reflux under a nitrogen atmosphere for 20 hr
  2. filtrationfiltered
  3. additionThe filtrate was treated with charcoal
  4. filtrationfiltered
  5. waitto stand at ambient temperature overnight
  6. filtrationfiltered
  7. washThe filter cake was washed with water, air
  8. customdried
  9. customrecrystallized from 2-propanol

出典と根拠

ORDレコード
ord-2198a4a148294a98bbb9e6b95d125ac7
出典データセット
uspto-grants-1990_02
特許番号
US04898874

反応ノート

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