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4-(1,1-Dimethylethoxycarbonyl)amino-3-methylphenoxyacetamide → 2-(4-Amino-3-methylphenoxy)acetamide

HRID 1584129
ノート
印刷プレビュー

反応式

HRID 1584129 の反応式
CC(C)(OC([NH:7][C:8]1[CH:18]=[CH:17][C:11]([O:12][CH2:13][C:14]([NH2:16])=[O:15])=[CH:10][C:9]=1[CH3:19])=O)C>FC(F)(F)C(O)=O>[NH2:7][C:8]1[CH:18]=[CH:17][C:11]([O:12][CH2:13][C:14]([NH2:16])=[O:15])=[CH:10][C:9]=1[CH3:19]
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

3

反応物 1

HCID 158708024-(1,1-Dimethylethoxycarbonyl)amino-3-methylphenoxyacetamide

生成物 1

HCID 158708032-(4-Amino-3-methylphenoxy)acetamide収率 50.7%

試薬・触媒・溶媒 1

HCID 6422Trifluoroacetic acid溶媒

反応条件

温度
0 °C

実験手順

To a 200 m1L round bottomed flask with a stirring bar and an argon inlet was added 4-(1,1-dimethylethoxycarbonyl)amino-3-methylphenoxyacetamide (4.91 g, 17.52 mmol) and trifluoroacetic acid (50 mL). This solution was stirred at 0° C. for 5 h. The trifluoroacetic acid was removed in vacuo and the residue was partitioned between EtOAc and aqueous NaHCO3 solution. The layers were separated and the organic phase was washed with brine, dried (MgSO4), filtered and concentrated in vacuo to give 1.60 g of 4-amino-3-methylphenoxy-acetamide as a white solid.

後処理

  1. customThe trifluoroacetic acid was removed in vacuo
  2. customthe residue was partitioned between EtOAc and aqueous NaHCO3 solution
  3. customThe layers were separated
  4. washthe organic phase was washed with brine
  5. dry with materialdried (MgSO4)
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-b35967b5bea747a38905af3f99a52b10
出典データセット
uspto-grants-1999_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05932582

反応ノート

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