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

HRID 854116
ノート
印刷プレビュー

反応式

HRID 854116 の反応式
[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]
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 80172-HydrazinoethanolHCID 198649192-Hydroxyimino-3-oxopropionitrile

生成物 1

HCID 1363755893-(2-Hydroxyethyl)hydrazono-2-hydroxyiminopropionitrile収率 99%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

反応条件

温度
5 °C

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-a3df4c264162493188a6bed6b7109c37
出典データセット
uspto-grants-2007_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07256304B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート