Reaktion #471568

ord-dc5fb015b817405ba46dc3b27b7b8d8a

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe reaction mixture was reacted at room temperature for 2 hours
  2. 2
    EinengenThe mixture was concentrated under reduced pressure
  3. 3
    WaschenThe resulting residue was washed with ethyl acetate (50 mL×3)
  4. 4
    Sonstigedried

Vorschrift

5-(3-Amino-2-methoxy-5-methyl-phenyl)-furan-2-carboxylic acid 46b (248 mg, 1 mmol) was dissolved in 20 mL of dichloromethane followed by dropwise addition of a solution of boron tribromide in dichloromethane (3 mL, 1 mmol/L). The reaction mixture was reacted at room temperature for 2 hours. The reaction was monitored by TLC until the disappearance of the starting materials. The mixture was concentrated under reduced pressure. The resulting residue was washed with ethyl acetate (50 mL×3) and dried to obtain the title compound 5-(3-amino-2-hydroxy-5-methyl-phenyl)-furan-2-carboxylic acid hydrobromide 46c (172 mg, yield 54.7%) as a white solid.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08367710B2uspto-grants-2013_02