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

HRID 1584129
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HRID 1584129 반응식
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]
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참가 물질

3

반응물 1

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

생성물 1

HCID 158708032-(4-Amino-3-methylphenoxy)acetamide수율 50.7%

시약·촉매·용매 1

HCID 6422Trifluoroacetic acid용매

반응 조건

온도
0 °C

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-b35967b5bea747a38905af3f99a52b10
출처 데이터셋
uspto-grants-1999_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05932582

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