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Ethanol → 4-Amino-5-fluoro-2-methoxybenzoic acid

HRID 630410
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HRID 630410 반응식
[NH2:1][C:2]1[C:9]([F:10])=[CH:8]C(C#N)=[C:4]([O:11][CH3:12])[CH:3]=1.[OH-:13].[Na+].[CH2:15]([OH:17])[CH3:16]>>[NH2:1][C:2]1[C:9]([F:10])=[CH:8][C:16]([C:15]([OH:13])=[O:17])=[C:4]([O:11][CH3:12])[CH:3]=1
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참가 물질

4

반응물 3

HCID 702EthanolHCID 14798Sodium HydroxideHCID 185196344-Amino-5-fluoro-2-methoxybenzonitrile2회

생성물 1

HCID 674693384-Amino-5-fluoro-2-methoxybenzoic acid수율 80%

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온도
110 °C

실험 절차

To a solution of 4-amino-5-fluoro-2-methoxybenzonitrile (intermediate 88; 5.3 g, 0.03 mol) in ethanol (20 mL) was added sodium hydroxide 8M (27.9 mL, 0.22 mol), the mixture was placed in a sealed vessel and heated to 110° C. for 20 hours. The solvent was removed under reduced pressure and the crude obtained was partitioned between water and ether. The aqueous layer was acidified by hydrochloric acid 6N until pH 4 and the crude was extracted with ethyl acetate, dried, filtered and evaporated under reduced pressure giving the title compound as a yellow solid (80%), which was used in the next step without further purification.

후처리

  1. customthe mixture was placed in a sealed vessel
  2. customThe solvent was removed under reduced pressure
  3. customthe crude obtained
  4. customwas partitioned between water and ether
  5. extractionthe crude was extracted with ethyl acetate
  6. customdried
  7. filtrationfiltered
  8. customevaporated under reduced pressure

출처 및 근거

ORD 기록
ord-b494ab6197e44209931d40c7e221138b
출처 데이터셋
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09315463B2

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