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

HRID 251959
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HRID 251959 반응식
[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]
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참가 물질

4

반응물 2

HCID 112312332-Amino-5-iodo-3-methylbenzoic AcidHCID 178418260HCID 178418260, 화합물

생성물 1

HCID 251569872-Amino-5-cyano-3-methylbenzoic acid수율 62.9%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

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온도
150 °C

실험 절차

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:

후처리

  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

출처 및 근거

ORD 기록
ord-c006a1f5e57347bfbc3b005969a7a53b
출처 데이터셋
uspto-grants-2011_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07867949B2

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