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2-Hydrazinoethanol → 3-(2-Hydroxyethyl)hydrazono-2-hydroxyiminopropionitrile

HRID 854116
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HRID 854116 반응식
[OH:1][N:2]=[C:3]([CH:6]=O)[C:4]#[N:5].[OH:8][CH2:9][CH2:10][NH:11][NH2:12]>CO>[OH:8][CH2:9][CH2:10][NH:11][N:12]=[CH:6][C:3](=[N:2][OH:1])[C:4]#[N:5]
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참가 물질

4

반응물 2

HCID 80172-HydrazinoethanolHCID 198649192-Hydroxyimino-3-oxopropionitrile

생성물 1

HCID 1363755893-(2-Hydroxyethyl)hydrazono-2-hydroxyiminopropionitrile수율 99%

시약·촉매·용매 1

HCID 887Methanol용매

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온도
5 °C

실험 절차

In a similar apparatus used in Example 1 were charged 0.98 g (10 mmol) of 2-hydroxyimino-3-oxopropionitrile synthesized by the same method as in Example 1 and 6 ml of methanol, and the mixture was cooled to 5° C. while stirring. Then, 0.80 g (10 mmol) of 95% by weight 2-hydroxyethylhydrazine was added to the mixture at the same temperature, and reacted at room temperature for 1 hour. After completion of the reaction, the reaction mixture was concentrated under reduced pressure, hexane was added to the concentrate, the resulting mixture was filtered and dried under reduced pressure to give 1.55 g (isolation yield: 99%) of 3-(2-hydroxyethyl)hydrazono-2-hydroxyiminopropionitrile as dark brownish solid.

후처리

  1. customreacted at room temperature for 1 hour
  2. customAfter completion of the reaction
  3. concentrationthe reaction mixture was concentrated under reduced pressure, hexane
  4. additionwas added to the concentrate
  5. filtrationthe resulting mixture was filtered
  6. customdried under reduced pressure

출처 및 근거

ORD 기록
ord-a3df4c264162493188a6bed6b7109c37
출처 데이터셋
uspto-grants-2007_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07256304B2

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