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Water → 4-Amino-2,5-difluorobenzoic acid

HRID 630422
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HRID 630422 반응식
[NH2:1][C:2]1[C:9]([F:10])=[CH:8][C:5]([C:6]#N)=[C:4]([F:11])[CH:3]=1.S(=O)(=O)(O)O.[OH2:17].[OH-:18].[Na+]>O1CCOCC1>[NH2:1][C:2]1[C:9]([F:10])=[CH:8][C:5]([C:6]([OH:18])=[O:17])=[C:4]([F:11])[CH:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962WaterHCID 1118Sulfuric AcidHCID 14798Sodium HydroxideHCID 27359004-Amino-2,5-difluorobenzonitrile

생성물 1

HCID 201514774-Amino-2,5-difluorobenzoic acid수율 42%

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

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이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트
온도
80 °C

실험 절차

To a solution of 4-amino-2,5-difluorobenzonitrile (6.21 g, 38.28 mmol) in dioxane (32.5 mL) was added 52.2 mL of sulphuric acid 73% p/p. The reaction mixture was stirred at 80° C. for 96 hours. The crude was poured into 250 mL of water and basified by sodium hydroxide 32% until basic pH and washed with methylen chloride. The aqueous phase was neutralized with hydrochloric acid 5N and the crude was extracted with ethyl acetate, washed with brine, dried and the solvent was removed under reduced pressure to give the title compound as a white solid (42%), which was used in the next step without further purification.

후처리

  1. washwashed with methylen chloride
  2. extractionthe crude was extracted with ethyl acetate
  3. washwashed with brine
  4. customdried
  5. customthe solvent was removed under reduced pressure

출처 및 근거

ORD 기록
ord-2b850a85c5434063a86781d4b90bc807
출처 데이터셋
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09315463B2

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