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Methanol → HCID 58085876, Verbindung

HRID 249827
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 249827
[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]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 3

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

Produkt 1

HCID 58085876HCID 58085876, VerbindungAusbeute 44 %

Reaktionsbedingungen

Temperatur
-78 °C

Versuchsvorschrift

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).

Aufarbeitung

  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)

Quellen und Nachweise

ORD-Eintrag
ord-05d52d7a71c7457ab0375c7cacfdf471
Quelldatensatz
uspto-grants-2011_01
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07863271B2

Notizen zur Reaktion

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