Potassium Hydroxide → alpha-[[(2,4,6-Trimethoxyphenyl)amino]carbonyl]benzene acetic acid

HRID 1938740Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1938740
[OH-].[K+].C([O:5][C:6](=[O:29])[CH:7]([C:14]([NH:16][C:17]1[C:22]([O:23][CH3:24])=[CH:21][C:20]([O:25][CH3:26])=[CH:19][C:18]=1[O:27][CH3:28])=[O:15])[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)C>C(O)C.O>[CH3:28][O:27][C:18]1[CH:19]=[C:20]([O:25][CH3:26])[CH:21]=[C:22]([O:23][CH3:24])[C:17]=1[NH:16][C:14]([CH:7]([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)[C:6]([OH:29])=[O:5])=[O:15]

Komponenten

5

Edukt 2

HCID 14797Potassium HydroxideHCID 10690735alpha-[[(2,4,6-Trimethoxyphenyl)amino]carbonyl] benzene acetic acid ethyl ester

Produkt 1

HCID 10665192alpha-[[(2,4,6-Trimethoxyphenyl)amino]carbonyl]benzene acetic acid

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 702EthanolLösungsmittelHCID 962WaterLösungsmittel

Versuchsvorschrift

To a stirred solution of KOH (10.70 g, 0.191 mol) in absolute ethanol (1.1 L) was added α-[[(2,4,6-trimethoxyphenyl)amino]carbonyl] benzene acetic acid ethyl ester (55.28 g, 0.1480 mol), and the mixture was stirred for 41 hours. The resulting suspension was diluted with H2O (~900 mL) and rotoevaporated to remove ethanol. The solution was washed (ethyl acetate) and acidified with dropwise addition of 1M HCl (265 mL). The resulting precipitate was filtered off, washed (H2O), and dried in vacuo to give an off-white solid; yield 48.4 g (100%); 111°-113° C. (gas evolution).

Aufarbeitung

  1. customto remove ethanol
  2. washThe solution was washed (ethyl acetate)
  3. additionacidified with dropwise addition of 1M HCl (265 mL)
  4. filtrationThe resulting precipitate was filtered off
  5. washwashed (H2O)
  6. customdried in vacuo
  7. customto give an off-white solid
  8. custom111°-113° C. (gas evolution)

Quellen und Nachweise

ORD-Eintrag
ord-00d64589d80e490f90656b58c8590c64
Quelldatensatz
uspto-grants-1997_12
Patentnummer
US05693657

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