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Methanol → HCID 58085876, 화합물

HRID 249827
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HRID 249827 반응식
[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]
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참가 물질

4

반응물 3

HCID 887MethanolHCID 24386Thionyl Chloride2회HCID 1514842-Amino-4-fluoro-3-hydroxybenzoic acid

생성물 1

HCID 58085876HCID 58085876, 화합물수율 44%

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온도
-78 °C

실험 절차

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).

후처리

  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)

출처 및 근거

ORD 기록
ord-05d52d7a71c7457ab0375c7cacfdf471
출처 데이터셋
uspto-grants-2011_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07863271B2

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