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Anthranilic Acid → 2-(Isopropylamino)benzoic acid

HRID 652303
ノート
印刷プレビュー

反応式

HRID 652303 の反応式
[C:1]([OH:10])(=[O:9])[C:2]1[C:3](=[CH:5][CH:6]=[CH:7][CH:8]=1)[NH2:4].[C:11](O)(=O)[C:12]1C(=CC=C[CH:20]=1)C(O)=O.[BH4-].[Na+]>CC(C)=O>[CH:12]([NH:4][C:3]1[C:2](=[CH:8][CH:7]=[CH:6][CH:5]=1)[C:1]([OH:10])=[O:9])([CH3:20])[CH3:11]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 227Anthranilic AcidHCID 1017Phthalic AcidHCID 4311764Sodium borohydride

生成物 1

HCID 122277122-(Isopropylamino)benzoic acid

試薬・触媒・溶媒 1

HCID 180Acetone溶媒

実験手順

To stirred mixture of 2.7 g. of anthranilic acid and 5.4 g. of phthalic acid in 23 ml. of acetone is added 0.7 g. of powdered sodium borohydride over a period of 30 minutes at 20° C.-30° C. The resulting slurry is then stirred at 35°-40° C. for 4 hours, diluted with 25 ml. of chloroform and filtered. The filtrate is concentrated in vacuo and the residue dissolved in 20 ml. of chloroform and treated with 30 ml. of hexane, filtered and the filtrate concentrated in vacuo to obtain a crude solid product which is recrystallized 5 times from cyclohexane to obtain (second crop of fifth recrystallization) N-isopropylanthranilic acid, m.p. 109°-109.5° C.

後処理

  1. additionmixture of 2.7 g
  2. stirringThe resulting slurry is then stirred at 35°-40° C. for 4 hours
  3. additiondiluted with 25 ml
  4. filtrationof chloroform and filtered
  5. concentrationThe filtrate is concentrated in vacuo
  6. dissolutionthe residue dissolved in 20 ml
  7. additionof chloroform and treated with 30 ml
  8. filtrationof hexane, filtered
  9. concentrationthe filtrate concentrated in vacuo
  10. customto obtain a crude solid product which
  11. customis recrystallized 5 times from cyclohexane

出典と根拠

ORDレコード
ord-da4aecf33b69426fad5521a1237919b9
出典データセット
uspto-grants-1987_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04670600

反応ノート

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