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Methanol → Methyl 2-fluoro-3-methylbenzoate

HRID 1866916
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1866916
[F:1][C:2]1[C:10]([CH3:11])=[CH:9][CH:8]=[CH:7][C:3]=1[C:4]([OH:6])=[O:5].S(=O)(=O)(O)O.[CH3:17]O>>[F:1][C:2]1[C:10]([CH3:11])=[CH:9][CH:8]=[CH:7][C:3]=1[C:4]([O:6][CH3:17])=[O:5]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 3

HCID 887MethanolHCID 1118Sulfuric AcidHCID 27373792-Fluoro-3-methylbenzoic acid

Produkt 1

HCID 22049929Methyl 2-fluoro-3-methylbenzoateAusbeute 82 %

Versuchsvorschrift

To a solution of 2-fluoro-3-methyl benzoic acid (3.57 g, 23 mmol) in MeOH (40 mL) was added concentrated sulfuric acid (2.3 mL), and the reaction mixture was heated at reflux for 12 h. The reaction mixture was cooled, the solvent was removed under reduced pressure, and the residue was dissolved in EtOAc. The organic solution was washed with a saturated solution of NaHCO3 and then brine, dried (Na2SO4), filtered and concentrated under reduced pressure to afford methyl 2 fluoro-3-methylbenzoate as a yellow oil (3.2 g, 82%): 1H NMR (300 MHz, CDCl3) δ 7.76-7.71 (m, 1H), 7.39-7.34 (m, 1H), 7.08 (t, J=8 Hz, 1H), 3.98 (s, 3H), 2.31 (d, J=3 Hz, 3H).

Aufarbeitung

  1. temperaturethe reaction mixture was heated
  2. temperatureat reflux for 12 h
  3. temperatureThe reaction mixture was cooled
  4. customthe solvent was removed under reduced pressure
  5. dissolutionthe residue was dissolved in EtOAc
  6. washThe organic solution was washed with a saturated solution of NaHCO3
  7. dry with materialbrine, dried (Na2SO4)
  8. filtrationfiltered
  9. concentrationconcentrated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-2c0230da45874d0db1f9d669bf94f7b7
Quelldatensatz
uspto-grants-2009_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07629363B2

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