Reacción #51772

ord-1598bca282c84c3d8e0b6d204eb7688d

Ecuación de reacción

Cc1ccc(C(C)(C)C)cc1[N+](=O)[O-]
4-tert-butyl-1-methyl-2-nitrobenzene
[K]
potassium
CCOCC
Et2O
CCOC(=O)C(=O)OCC
diethyl oxalate
CCOC(=O)C(=O)Cc1ccc(C(C)(C)C)cc1[N+](=O)[O-]
title compound
CCOC(=O)C(=O)Cc1ccc(C(C)(C)C)cc1[N+](=O)[O-]
3-(4-tert-Butyl-2-nitro-phenyl)-2-oxo-propionic acid ethyl ester

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Procedimiento

The title compound was prepared by adapting the procedure described by Gagliardi S., et al., in J. Med. Chem., 1998;41:1568 using potassium (1.66 g, 42.4 mmol), Et2O (200 mL), EtOH (10 mL), diethyl oxalate (7.56 g, 51.8 mmol), and 4-tert-butyl-1-methyl-2-nitrobenzene (prepared in Example WW; 10.0 g, 51.8 mmol). MS(APCI): 294 (M+H).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06852711B2uspto-grants-2005_02