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

HRID 2363805
ノート
印刷プレビュー

反応式

HRID 2363805 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 1

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

生成物 1

HCID 823722636-Fluoro-4-hydroxy-2-naphthoic acid収率 71.7%

試薬・触媒・溶媒 1

HCID 62406Trifluoromethanesulfonic acid溶媒

実験手順

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.

後処理

このページの内容参加物実験手順後処理出典と根拠反応ノート
addition
The resulting mixture was carefully poured into ice cold water
  • customto obtain a solid precipitate, which
  • filtrationwas filtered
  • washwashed with water
  • customdried under vacuum
  • 出典と根拠

    ORDレコード
    ord-e16fbc208e1e4561ad5f9a4e0a736a21
    出典データセット
    uspto-grants-2014_04
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US08691993B2

    反応ノート

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