Reaction #7195

ord-9da17a98ecc54954bc7c708f1d2b6ac4

Reaction equation

COc1ccc(-c2c[nH]cn2)cc1
4-(4-methoxyphenyl)-1H-imidazole
[H-].[Na+]
NaH
C[Si](C)(C)CCOCCl
SEMCl
COc1ccc(-c2cn(COCC[Si](C)(C)C)cn2)cc1
title compound
Yield 64.0%
COc1ccc(-c2cn(COCC[Si](C)(C)C)cn2)cc1
4-(4-Methoxyphenyl)-1-(2-trimethylsilanyl-ethoxymethyl)-1H-imidazole
Yield 64.0%

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Procedure

Reaction of 4-(4-methoxyphenyl)-1H-imidazole (610 mg, 3.51 mmol), NaH (60%, 136 mg, 3.40 mmol), and SEMCl (656 uL, 3.71 mmol) followed by column chromatography on silica gel (hexane/EtOAC 1:1) gave the title compound (654 mg, 64%) as a yellow solid. 1H NMR (300 MHz, CDCl3) major isomer: δ 0.00 (s, 9H), 0.93 (t, 2H, J=7.5 Hz), 3.52 (t, 2H, J=7.5 Hz), 3.83 (s, 3H), 5.28 (s, 2H), 6.94 (d, 2H, J=9.0 Hz), 7.24 (s, 1H), 7.60 (s, 1H), 7.72 (d, 2H, J=9.0 Hz); minor isomer: δ 0.00 (s, 9H), 0.92 (t, 2H, J=7.5 Hz), 3.54 (t, 2H, J=7.5 Hz), 3.85 (s, 3H), 5.23 (s, 2H), 6.98 (d, 2H, J=9.0 Hz), 7.09 (s, 1H), 7.47 (d, 2H, J=9.0 Hz), 7.65 (s, 1H). ES-MS m/z 305 (M+H).

Source

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