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Methanol → HCID 58085876、化合物

HRID 249827
ノート
印刷プレビュー

反応式

HRID 249827 の反応式
[NH2:1][C:2]1[C:10]([OH:11])=[C:9]([F:12])[CH:8]=[CH:7][C:3]=1[C:4]([OH:6])=[O:5].S(Cl)(Cl)=O.[CH3:17]O>>[NH2:1][C:2]1[C:10]([OH:11])=[C:9]([F:12])[CH:8]=[CH:7][C:3]=1[C:4]([O:6][CH3:17])=[O:5]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 3

HCID 887MethanolHCID 24386Thionyl Chloride2 回HCID 1514842-Amino-4-fluoro-3-hydroxybenzoic acid

生成物 1

HCID 58085876HCID 58085876、化合物収率 44%

反応条件

温度
-78 °C

実験手順

To a solution of 2-amino-4-fluoro-3-hydroxybenzoic acid (2.44 g, 9.7 mmol) in methanol (200 mL) was added thionyl chloride (3.8 mL, 50 mmol) at −78° C. The mixture was stirred in the boiling solvent for 17 h. The solvent was removed under reduced pressure; the residue was dissolved in methanol (200 mL). The solution was cooled to −78° C. and treated with thionyl chloride (8 mL, 100 mmol). The mixture was stirred in boiling solvent for 48 h. The solvent was removed under reduced pressure and the crude material was purified by column chromatography (silica gel, 0 to 70% ethyl acetate in hexanes) to afford methyl 2-amino-4-fluoro-3-hydroxybenzoate (1.5 g, 44%) as off-white solid. 1H NMR (300 MHz, CDCl3) δ 7.48-7.43 (m, 1H), 6.40 (t, J=9.3 Hz, 1H), 3.87 (s, 3H); MS (ESI+) m/z 186 (M+H).

後処理

  1. customThe solvent was removed under reduced pressure
  2. dissolutionthe residue was dissolved in methanol (200 mL)
  3. stirringThe mixture was stirred
  4. customfor 48 h
  5. customThe solvent was removed under reduced pressure
  6. customthe crude material was purified by column chromatography (silica gel, 0 to 70% ethyl acetate in hexanes)

出典と根拠

ORDレコード
ord-05d52d7a71c7457ab0375c7cacfdf471
出典データセット
uspto-grants-2011_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07863271B2

反応ノート

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