Reaction #7196

ord-f76d24e594c14444b92e85c37f612993

Reaction equation

O=[N+]([O-])c1ccc(-c2c[nH]cn2)cc1
4-(4-nitrophenyl)-1H-imidazole
[H-].[Na+]
NaH
C[Si](C)(C)CCOCCl
SEMCl
C[Si](C)(C)CCOCn1cncc1-c1ccc([N+](=O)[O-])cc1
title compound
Yield 65.0%
C[Si](C)(C)CCOCn1cncc1-c1ccc([N+](=O)[O-])cc1
5-(4-Nitrophenyl)-1-(2-trimethylsilanyl-ethoxymethyl)-1H-imidazole
Yield 65.0%

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Procedure

Reaction of 4-(4-nitrophenyl)-1H-imidazole (160 mg, 0.85 mmol), NaH (60%, 33 mg, 0.82 mmol), and SEMCl (158 uL, 0.89 mmol) followed by column chromatography on silica gel (hexane/EtOAC 3:2) gave the title compound (170 mg, 65%) as a yellow solid. 1H NMR (300 MHz, CDCl3) δ 0.00 (s, 9H), 0.94 (t, 2H, J=7.5 Hz), 3.55 (t, 2H, J=7.5 Hz), 5.33 (s, 2H), 7.50 (s, 1H), 7.69 (s, 1H), 7.94 (d, 2H, J=6.0 Hz), 8.26 (d, 2H, J=6.0 Hz).

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07084155B2uspto-grants-2006_08