Methanol → Methyl 3-hydroxy-2-nitrobenzoate

HRID 415162

Reaktionsgleichung

Reaktionsgleichung von HRID 415162
[OH:1][C:2]1[C:3]([N+:11]([O-:13])=[O:12])=[C:4]([CH:8]=[CH:9][CH:10]=1)[C:5]([OH:7])=[O:6].OS(O)(=O)=O.[CH3:19]O>>[OH:1][C:2]1[C:3]([N+:11]([O-:13])=[O:12])=[C:4]([CH:8]=[CH:9][CH:10]=1)[C:5]([O:7][CH3:19])=[O:6]

Komponenten

4

Edukt 3

HCID 887MethanolHCID 1118Sulfuric AcidHCID 2932913-Hydroxy-2-nitrobenzoic acid

Produkt 1

HCID 13659833Methyl 3-hydroxy-2-nitrobenzoate

Versuchsvorschrift

A solution of 3-hydroxy-2-nitrobenzoic acid (51 g) and con.H2SO4 (5 mL) in anhydrous methanol (450 mL) was heated to reflux for 48 hr. The mixture was concentrated to remove methanol, and the residue was partitioned between water (500 mL) and ethyl acetate (800 mL). The organic layer was washed with brine (300 mL), dried over anhydrous sodium sulfate, and concentrated to give crude compound. The crude product was purified by chromatography (silica gel, petroleum ether/ethyl acetate=40:1 to 5:1) to give methyl 3-hydroxy-2-nitrobenzoate (28 g) 1H-NMR (400 MHz, CDCl3) δ 3.8 (s, 3H), 7.32-7.34 (d, J=8.4 Hz, 1H), 7.39-7.41 (d, J=8.0 Hz, 1H), 7.48-7.52 (t, J=8.0 Hz, 1H), 11.37 (s, 1H); LC-MS (m/z) 198 [M+1]+.

Aufarbeitung

  1. temperatureto reflux for 48 hr
  2. concentrationThe mixture was concentrated
  3. customto remove methanol
  4. customthe residue was partitioned between water (500 mL) and ethyl acetate (800 mL)
  5. washThe organic layer was washed with brine (300 mL)
  6. dry with materialdried over anhydrous sodium sulfate
  7. concentrationconcentrated
  8. customto give crude compound
  9. customThe crude product was purified by chromatography (silica gel, petroleum ether/ethyl acetate=40:1 to 5:1)

Quellen und Nachweise

ORD-Eintrag
ord-898faeee71a3496982246edc800080a2
Quelldatensatz
uspto-grants-2012_01
Patentnummer
US08088760B2

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