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Sodium Hydroxide → Bis(4-methylphenyl)azidoacetic acid

HRID 2304574
ノート
印刷プレビュー

反応式

HRID 2304574 の反応式
[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([C:16]2[CH:21]=[CH:20][C:19]([CH3:22])=[CH:18][CH:17]=2)([N:13]=[N+:14]=[N-:15])[C:9]([O:11]C)=[O:10])=[CH:4][CH:3]=1.[OH-].[Na+]>O1CCCC1>[CH3:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]([C:16]2[CH:17]=[CH:18][C:19]([CH3:22])=[CH:20][CH:21]=2)([N:13]=[N+:14]=[N-:15])[C:9]([OH:11])=[O:10])=[CH:6][CH:7]=1
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 14798Sodium HydroxideHCID 18435794Methyl bis(4-methylphenyl)azidoacetate

生成物 1

HCID 18435787Bis(4-methylphenyl)azidoacetic acid

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

To a solution of methyl bis(4-methylphenyl)azidoacetate (2.07 g, 7.01 mmol) in tetrahydrofuran(15 mL) was added 2 M aqueous sodium hydroxide (3.86 ml, 7.71 mmol). The mixture was stirred at room temperature for 18 hours, and then the solvents were removed in vacuo. The residue was dissolved in ethyl acetate and washed with 1M HCl and brine. The organic layer was dried over sodium sulfate, filtered and concentrated to give the title compound as a waxy solid which was used as is.

後処理

  1. customthe solvents were removed in vacuo
  2. dissolutionThe residue was dissolved in ethyl acetate
  3. washwashed with 1M HCl and brine
  4. dry with materialThe organic layer was dried over sodium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated

出典と根拠

ORDレコード
ord-57b8c2403f904751a4f2b17a1e240004
出典データセット
uspto-grants-2002_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06436962B1

反応ノート

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