Methanol → Benzoic acid, 3-(aminosulfonyl)-, methyl ester

HRID 331188

Reaktionsgleichung

Reaktionsgleichung von HRID 331188
[NH2:1][S:2]([C:5]1[CH:6]=[C:7]([CH:11]=[CH:12][CH:13]=1)[C:8]([OH:10])=[O:9])(=[O:4])=[O:3].S(Cl)(Cl)=O.[CH3:18]O>>[NH2:1][S:2]([C:5]1[CH:6]=[C:7]([CH:11]=[CH:12][CH:13]=1)[C:8]([O:10][CH3:18])=[O:9])(=[O:3])=[O:4]

Komponenten

4

Edukt 3

HCID 887MethanolHCID 24386Thionyl ChlorideHCID 2293523-Sulfamoylbenzoic acid

Produkt 1

HCID 108836Benzoic acid, 3-(aminosulfonyl)-, methyl esterAusbeute 73 %

Versuchsvorschrift

To a solution of 3-(aminosulfonyl)benzoic acid (22 g, 0.109 mol) in MeOH (250 ml) is added thionyl chloride (25 ml, 0.328 mol) and the mixture is refluxed for 16 h. The solvent is removed and the residue is diluted with EtOAc (200 ml), washed with a 10% solution of sodium bicarbonate, water and brine. The solvent was removed under vacuum to afford 17 g (73%) of the title compound as a solid. 1H NMR (DMSO-d6) δ 8.39 (t, J=1.5 Hz, 1H), 8.16-8.13 (m, 1H), 8.09-8.05 (m, 1H), 7.76 (t, J=7.9 Hz, 1H), 7.53 (s, 2H), 3.90 (s, 3H). HPLC (max plot) 99%; Rt 1.49 min. LC/MS: (ES+):215.9, (ES−):214.1.

Aufarbeitung

  1. temperaturethe mixture is refluxed for 16 h
  2. customThe solvent is removed
  3. additionthe residue is diluted with EtOAc (200 ml)
  4. washwashed with a 10% solution of sodium bicarbonate, water and brine
  5. customThe solvent was removed under vacuum

Quellen und Nachweise

ORD-Eintrag
ord-906813f66a2b49e89bf0d203116b5627
Quelldatensatz
uspto-grants-2014_11
Patentnummer
US08877757B2

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