Reaction #731583

ord-eab15355bce64c8bbc10a08fb4923ec7

Reaction equation

CCO
Ethanol
N#Cc1ccc(OCc2ccccc2)c(C(=O)OCc2ccccc2)c1
2-benzyloxy-5-cyanobenzoic acid benzyl ester
N#Cc1ccc(O)c(C(=O)O)c1
title compound
Yield 100.0%
N#Cc1ccc(O)c(C(=O)O)c1
5-Cyanosalicylic acid
Yield 100.0%

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    FiltrationAfter the insoluble matter was filtered off
  2. 2
    Otherthe solvent was evaporated under reduced pressure

Procedure

Ethanol (10 mL) and tetrahydrofuran (10 mL) were added to 2-benzyloxy-5-cyanobenzoic acid benzyl ester (446 mg, 1.3 mmol) and 5% palladium on carbon (45 mg), and the mixture was hydrogenated at room temperature for 2 hours. After the insoluble matter was filtered off, the solvent was evaporated under reduced pressure to give the title compound (212 mg, 100.0%) as a white solid.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07700655B2uspto-grants-2010_04