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Sodium Hydroxide → N-(3-phenyl-isoxazol-5-yl)-malonamic acid

HRID 1665682
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반응식

HRID 1665682 반응식
[OH-].[Na+].C([O:5][C:6](=[O:22])[CH2:7][C:8]([NH:10][C:11]1[O:15][N:14]=[C:13]([C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)[CH:12]=1)=[O:9])C>C1COCC1.O>[C:16]1([C:13]2[CH:12]=[C:11]([NH:10][C:8](=[O:9])[CH2:7][C:6]([OH:22])=[O:5])[O:15][N:14]=2)[CH:17]=[CH:18][CH:19]=[CH:20][CH:21]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 14798Sodium HydroxideHCID 57875820N-(3-phenyl-isoxazol-5-yl)-malonamic acid ethyl ester

생성물 1

HCID 57875817N-(3-phenyl-isoxazol-5-yl)-malonamic acid수율 65.3%

시약·촉매·용매 2

HCID 962Water용매HCID 8028Tetrahydrofuran용매

실험 절차

NaOH (57 mg, 1.4 mmol) was added to a stirred solution of N-(3-phenyl-isoxazol-5-yl)-malonamic acid ethyl ester (78 mg, 0.28 mmol) in a mixture of THF (12 mL) and H2O (12 mL) and stirring was continued at ambient temperature overnight. The reaction mixture was concentrated. The residue was diluted with water, washed with diethyl ether, acidified with concentrated HCl. The precipitate was filtered to afford 45 mg (64.28% Yield) of N-(3-phenyl-isoxazol-5-yl)-malonamic acid.

후처리

  1. concentrationThe reaction mixture was concentrated
  2. additionThe residue was diluted with water
  3. washwashed with diethyl ether
  4. filtrationThe precipitate was filtered

출처 및 근거

ORD 기록
ord-b2c7b3e1e0c74e5d9926245c2ec3be91
출처 데이터셋
uspto-grants-2011_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08039463B2

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