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2-[1-(4-fluoro-phenyl)-meth-(E)-ylidene]-succinic acid → 6-Fluoro-4-hydroxy-2-naphthoic acid

HRID 2363805
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인쇄 미리보기

반응식

HRID 2363805 반응식
[F:1][C:2]1[CH:7]=[CH:6][C:5](/[CH:8]=[C:9](\[CH2:13][C:14]([OH:16])=O)/[C:10]([OH:12])=[O:11])=[CH:4][CH:3]=1>FC(F)(F)S(O)(=O)=O>[F:1][C:2]1[CH:3]=[C:4]2[C:5](=[CH:6][CH:7]=1)[CH:8]=[C:9]([C:10]([OH:12])=[O:11])[CH:13]=[C:14]2[OH:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 821588632-[1-(4-fluoro-phenyl)-meth-(E)-ylidene]-succinic acid

생성물 1

HCID 823722636-Fluoro-4-hydroxy-2-naphthoic acid수율 71.7%

시약·촉매·용매 1

HCID 62406Trifluoromethanesulfonic acid용매

실험 절차

A solution of 2-[1-(4-fluoro-phenyl)-meth-(E)-ylidene]-succinic acid (0.100 g, 0.44 mmol) in trifluoromethanesulfonic acid (0.5 mL) was stirred at room temperature for 16 hours. The resulting mixture was carefully poured into ice cold water with continuous stirring to obtain a solid precipitate, which was filtered, washed with water and dried under vacuum to yield 6-fluoro-4-hydroxy-naphthalene-2-carboxylic acid (0.065 g, 71%) as yellow solid. This crude product was pure enough to proceed to next step without further purification.

후처리

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  • additionThe resulting mixture was carefully poured into ice cold water
  • customto obtain a solid precipitate, which
  • filtrationwas filtered
  • washwashed with water
  • customdried under vacuum
  • 출처 및 근거

    ORD 기록
    ord-e16fbc208e1e4561ad5f9a4e0a736a21
    출처 데이터셋
    uspto-grants-2014_04
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US08691993B2

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