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Sodium Hypochlorite → 2-methoxyethyl N-(2-methoxyethoxycarbonylimino)carbamate

HRID 1162861
ノート
印刷プレビュー

反応式

HRID 1162861 の反応式
[CH3:1][O:2][CH2:3][CH2:4][O:5][C:6]([NH:8][NH:9][C:10]([O:12][CH2:13][CH2:14][O:15][CH3:16])=[O:11])=[O:7].Cl[O-].[Na+]>C1(C)C=CC=CC=1>[CH3:1][O:2][CH2:3][CH2:4][O:5][C:6]([N:8]=[N:9][C:10]([O:12][CH2:13][CH2:14][O:15][CH3:16])=[O:11])=[O:7]
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 2

HCID 23665760Sodium HypochloriteHCID 249880741,2-Bis(2-methoxyethyl) 1,2-hydrazinedicarboxylate

生成物 1

HCID 533844152-methoxyethyl N-(2-methoxyethoxycarbonylimino)carbamate収率 37%

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

実験手順

To a solution obtained by adding 1,2-hydrazinedicarboxylic acid bis(2-methoxyethyl) ester (200 mg, 0.85 mmol) and toluene (2 mL) to a 10 mL flask, followed by cooling with an ice bath, was added dropwise a 5% sodium hypochlorite solution (1.39 g, 0.85 mmol), and the reaction was allowed to proceed for one hour. After the reaction, the solution was washed with water (1 mL,×2), and dehumidified with anhydrous magnesium sulfate, followed by concentration to dryness. The resulting solid was recrystallized with toluene (1 mL) and hexane (5 mL), to give azodicarboxylic acid bis(2-methoxyethyl) ester as a pale yellow crystal (73 mg, yield: 37%).

後処理

  1. customTo a solution obtained
  2. temperatureby cooling with an ice bath
  3. customAfter the reaction
  4. washthe solution was washed with water (1 mL,×2)
  5. concentrationfollowed by concentration to dryness
  6. customThe resulting solid was recrystallized with toluene (1 mL) and hexane (5 mL)

出典と根拠

ORDレコード
ord-dd658f41e03f4141823a407a8c7c62db
出典データセット
uspto-grants-2010_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07820802B2

反応ノート

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