Reaktion #417941

ord-1eb8cd1d69e04211956f80992d8ed9cc

Reaktionsgleichung

O=C([O-])O.[Na+]
NaHCO3
COC(=O)c1ccc(O)c(N)c1
methyl 3-amino-4-hydroxybenzoate
COC(=O)c1ccc(C=O)cc1
methyl 4-formylbenzoate
N#CC1=C(C#N)C(=O)C(Cl)=C(Cl)C1=O
DDQ
CCOC(=O)c1ccc(N)c(N)c1
compound 1
Ausbeute 86.0%
CCOC(=O)c1ccc(N)c(N)c1
3,4-diamino-benzoic acid ethyl ester
Ausbeute 86.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe solvent was evaporated under reduced pressure
  2. 2
    workup.DISSOLUTIONthe remaining residue was dissolved in dichloromethane (150 mL)
  3. 3
    workup.STIRRINGthe reaction mixture was stirred at rt for 1 h
  4. 4
    FiltrationThe suspension was filtered off
  5. 5
    Waschenthe resulting solid was washed with saturated NaHCO3 (50 mL), water (50 mL), and ethyl acetate (100 mL)
  6. 6
    Sonstigedried in vacuo

Vorschrift

A mixture of methyl 3-amino-4-hydroxybenzoate (2.5 g, 15 mmol) and methyl 4-formylbenzoate (2.46 g, 15 mmol) in methanol (75 mL) was stirred at rt overnight. The solvent was evaporated under reduced pressure and the remaining residue was dissolved in dichloromethane (150 mL). DDQ (3.5 g, 15.4 mmol) was added and the reaction mixture was stirred at rt for 1 h. Saturated NaHCO3 (200 mL) was added. The suspension was filtered off, the resulting solid was washed with saturated NaHCO3 (50 mL), water (50 mL), and ethyl acetate (100 mL) and dried in vacuo to give compound 1 (4 g, 86% yield) as yellow solid.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08877707B2uspto-grants-2014_11