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2-(4-Amino-3-methylphenoxy)ethan-1-ol → Ethyl 2-{[4-(2-hydroxyethoxy)-2-methylphenyl]amino}-4-oxo-4,5-dihydrofuran-3-carboxylate

HRID 402641
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HRID 402641 반응식
[OH:1][CH2:2][CH2:3][O:4][C:5]1[CH:11]=[CH:10][C:8]([NH2:9])=[C:7]([CH3:12])[CH:6]=1.C(O[C:16]1[O:17][CH2:18][C:19](=[O:26])[C:20]=1[C:21]([O:23][CH2:24][CH3:25])=[O:22])C>C(O)C>[OH:1][CH2:2][CH2:3][O:4][C:5]1[CH:11]=[CH:10][C:8]([NH:9][C:16]2[O:17][CH2:18][C:19](=[O:26])[C:20]=2[C:21]([O:23][CH2:24][CH3:25])=[O:22])=[C:7]([CH3:12])[CH:6]=1
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참가 물질

4

반응물 2

HCID 4592592-(4-Amino-3-methylphenoxy)ethan-1-olHCID 13791062Ethyl 2-ethoxy-4-oxo-4,5-dihydrofuran-3-carboxylate

생성물 1

HCID 86708330Ethyl 2-{[4-(2-hydroxyethoxy)-2-methylphenyl]amino}-4-oxo-4,5-dihydrofuran-3-carboxylate

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A solution of 4-(2-hydroxyethoxy)-2-methylaniline (0.69 g, 4.1 mmol) and ethyl 2-ethoxy-4-oxo-4,5-dihydrofuran-3-carboxylate (0.83 g, 4.2 mmol) in ethanol (8.3 mL) was stirred at ambient temperature for 16 h. The solvent was removed under reduced pressure, and ethanol was added to precipitate the product. The precipitate was collected by filtration then dried to afford ethyl 2-{[4-(2-hydroxyethoxy)-2-methylphenyl]amino}-4-oxo-4,5-dihydrofuran-3-carboxylate as solid (0.55 g, y. 42%).

후처리

  1. customThe solvent was removed under reduced pressure, and ethanol
  2. additionwas added
  3. customto precipitate the product
  4. filtrationThe precipitate was collected by filtration
  5. customthen dried

출처 및 근거

ORD 기록
ord-c3e10ebeaaae4ecd8bcafe53c4dc3358
출처 데이터셋
uspto-grants-2014_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08742113B2

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