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2-Amino-5-iodo-3-methylbenzoic Acid → 2-Amino-5-cyano-3-methylbenzoic acid

HRID 251959
ノート
印刷プレビュー

反応式

HRID 251959 の反応式
[NH2:1][C:2]1[C:10]([CH3:11])=[CH:9][C:8](I)=[CH:7][C:3]=1[C:4]([OH:6])=[O:5].[Cu](C#N)[C:14]#[N:15]>CN(C)C=O>[NH2:1][C:2]1[C:10]([CH3:11])=[CH:9][C:8]([C:14]#[N:15])=[CH:7][C:3]=1[C:4]([OH:6])=[O:5]
参加物反応条件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 112312332-Amino-5-iodo-3-methylbenzoic AcidHCID 178418260HCID 178418260、化合物

生成物 1

HCID 251569872-Amino-5-cyano-3-methylbenzoic acid収率 62.9%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

反応条件

温度
150 °C

実験手順

A mixture of 1.0 g of 2-amino-5-iodo-3-methylbenzoic acid, 0.45 g of copper cyanide and 10 ml of N,N-dimethylformamide was stirred at 150° C. for 9 hours. The reaction mixture was concentrated under reduced pressure. Into the residue, 20 ml of water and 2 ml of ethylenediamine were poured, and the mixture was stirred at room temperature for 1 hour. After the reaction mixture was filtered, the filtrate was adjusted to around pH 5 by an addition of concentrated hydrochloric acid, and then extracted with ethyl acetate three times. The combined organic layer was dried over sodium sulfate, and concentrated under reduced pressure to obtain 0.40 g of 2-amino-5-cyano-3-methylbenzoic acid of the formula:

後処理

  1. concentrationThe reaction mixture was concentrated under reduced pressure
  2. additionInto the residue, 20 ml of water and 2 ml of ethylenediamine were poured
  3. stirringthe mixture was stirred at room temperature for 1 hour
  4. filtrationAfter the reaction mixture was filtered
  5. additionthe filtrate was adjusted to around pH 5 by an addition of concentrated hydrochloric acid
  6. extractionextracted with ethyl acetate three times
  7. dry with materialThe combined organic layer was dried over sodium sulfate
  8. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-c006a1f5e57347bfbc3b005969a7a53b
出典データセット
uspto-grants-2011_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07867949B2

反応ノート

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