Reaktion #2298613

ord-cf0ed24154e14f5f9a947583dc6bd10b

Reaktionsgleichung

CC(=O)OC(C)=O
acetic anhydride
COC(=O)c1sc(C)c(C)c1N
methyl 3-amino-4-methyl-2-thiophenecarboxylic acid methyl ester
COC(=O)c1scc(C)c1NC=O
3-(formylamino)-4-methyl-2-thiophenecarboxylic acid methyl ester
Ausbeute 95.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturwhile cooling in an ice bath
  2. 2
    SonstigeThe cooling bath was removed
  3. 3
    workup.ADDITIONThe reaction mixture was diluted with water (100 mL)
  4. 4
    Filtrationthe solid product collected by vacuum filtration

Vorschrift

Formic acid (53 mL) was added to acetic anhydride (53 mL) while cooling in an ice bath. Solid methyl 3-amino-4-methyl-2-thiophenecarboxylic acid methyl ester (1, 18.2 g, 0.11 mol) was added to the cold solution in small portions. The cooling bath was removed and the resulting suspension was stirred at room temperature for 4 hours. The reaction mixture was diluted with water (100 mL) and the solid product collected by vacuum filtration to yield 3-(formylamino)-4-methyl-2-thiophenecarboxylic acid methyl ester (20.2 g, 95% yield) as a white solid.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: USRE039267E1uspto-grants-2006_09