Reaktion #412245

ord-614a87542aed44478558343a40daeec6

Reaktionsgleichung

COC(=O)c1ccc2cc(C#N)ccc2c1
6-cyano-naphthalene-2-carboxylic acid methyl ester
COC(=O)c1ccc2cc(C#N)ccc2c1
6-Cyano-naphthalene-2-carboxylic acid methyl ester
[Li+].[OH-]
LiOH
N#Cc1ccc2cc(C(=O)O)ccc2c1
desired compound
Ausbeute 86.2%
N#Cc1ccc2cc(C(=O)O)ccc2c1
6-Cyano-naphthalene-2-carboxylic acid
Ausbeute 86.2%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Extraktionextracted with EtOAc (2×150 mL)
  2. 2
    Trocknenextracts dried over MgSO4
  3. 3
    Einengenconcentrated

Vorschrift

A solution of 6-cyano-naphthalene-2-carboxylic acid methyl ester from Example 96 (2.00 g, 9.47 mmol) in THF (19 mL) and 1M aqueous LiOH (18.94 mL, 18,94 mmol) was vigorously stirred at room temperature for 3 hours. The reaction mixture was then diluted with 150 mL of 1:1 dichloromethane/water, and the organics were discarded. The aqueous material was acidified to pH 2 with 1N HC1, extracted with EtOAc (2×150 mL), extracts dried over MgSO4, and concentrated to provide the desired compound as a white solid (1.61 g, 86%).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06221914B1uspto-grants-2001_04