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1-Butanol → Anthranilic acid, 5-chloro-, butyl ester

HRID 2163567
ノート
印刷プレビュー

反応式

HRID 2163567 の反応式
[CH3:1][O:2][C:3](=[O:12])[C:4]1[C:5](=[CH:7][CH:8]=[C:9]([Cl:11])[CH:10]=1)[NH2:6].C(=O)([O-])[O-].[K+].[K+].[CH2:19](O)[CH2:20][CH2:21]C>>[CH2:1]([O:2][C:3](=[O:12])[C:4]1[C:5](=[CH:7][CH:8]=[C:9]([Cl:11])[CH:10]=1)[NH2:6])[CH2:19][CH2:20][CH3:21]
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 3

HCID 2631-ButanolHCID 11430Potassium CarbonateHCID 78878Methyl 2-amino-5-chlorobenzoate

生成物 1

HCID 140347Anthranilic acid, 5-chloro-, butyl ester収率 93%

実験手順

186 parts of 5-chloroanthranilic acid methyl ester, 150 parts of n-butanol and 10 parts of potassium carbonate are refluxed for half an hour. The separated methanol is then distilled off over a column. Distillation is continued until the boiling point of n-butanol is reached, then after addition of 4 parts each of bleaching earth and of active charcoal the hot mixture is filtered and agitated with 100 parts of acetone and 200 parts of ice. The reaction lasts for about 6 hours. The precipitate is filtered off, washed with ice-cold water and dried in vacuo at room temperature. There are obtained 211 parts of 5-chloroanthranilic acid-n-butyl ester, melting point 37°-39° C. The yield is 93% of the theory.

後処理

  1. distillationThe separated methanol is then distilled off over a column
  2. distillationDistillation
  3. additionafter addition of 4 parts
  4. filtrationof active charcoal the hot mixture is filtered
  5. filtrationThe precipitate is filtered off
  6. washwashed with ice-cold water
  7. customdried in vacuo at room temperature

出典と根拠

ORDレコード
ord-c36bbca07b6848d8b66df8ad5925dcdb
出典データセット
uspto-grants-1979_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04135050

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート