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Ammonium Hydroxide → HCID 54549569、化合物

HRID 1504950
ノート
印刷プレビュー

反応式

HRID 1504950 の反応式
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][CH2:9][CH2:10][C:11]([O:13]C)=O)=[CH:4][CH:3]=1.[NH4+:15].[OH-]>CO>[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][CH2:9][CH2:10][C:11]([NH2:15])=[O:13])=[CH:4][CH:3]=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 14923Ammonium HydroxideHCID 88628Methyl 4-aminobenzenebutanoate

生成物 1

HCID 54549569HCID 54549569、化合物収率 70%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

To a solution of compound 27 (300 mg, 1.55 mmol) in CH3OH (5 mL) was added NH4OH (32) at room temperature with stirring. The reaction mixture was stirred at room temperature for 6 h and concentrated in vacuo. The residue was diluted with water and extracted with DCM/CH3OH (10:1). The combined organic layers were dried over Na2SO4 and concentrated to dryness to give compound 33 (194 mg, 70%) as a white solid. The crude product was used directly for the next step without purification.

後処理

  1. stirringThe reaction mixture was stirred at room temperature for 6 h
  2. concentrationconcentrated in vacuo
  3. additionThe residue was diluted with water
  4. extractionextracted with DCM/CH3OH (10:1)
  5. dry with materialThe combined organic layers were dried over Na2SO4
  6. concentrationconcentrated to dryness

出典と根拠

ORDレコード
ord-dfc911b0f96a4bae878ba53802b70ee4
出典データセット
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09216957B2

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート