反応 #7286

ord-9c09c4ea714e44078cb8dba8f34d5adb

反応方程式

C[Si](C)(C)CCOCCl
2-(trimethylsilyl)ethoxymethyl chloride
c1ccc2[nH]cnc2c1
benzimidazole
CCN(C(C)C)C(C)C
N,N-diisopropylethylamine
CN(C)C=O
DMF
C[Si](C)(C)CCOCn1c(C=O)nc2ccccc21
1-(2-trimethylsilylethoxymethyl)-benzimidazole
収率 76.0%
C[Si](C)(C)CCOCn1c(C=O)nc2ccccc21
1-[[2-(trimethylsilyl)ethoxy]methyl]-benzimidazole-2-carboxaldehyde
収率 76.0%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他Purification of the crude brown oil through a plug of silica gel (CH2Cl2/MeOH, 19:1)

実験手順

To a stirred solution of benzimidazole (2.00 g, 16.9 mmol) in anhydrous DMF (25 mL) was added N,N-diisopropylethylamine (7.3 mL, 42.2 mmol) followed by 2-(trimethylsilyl)ethoxymethyl chloride (3.3 mL, 18.6 mmol) and the resultant solution was heated to 80□ C. for 4 hours. Purification of the crude brown oil through a plug of silica gel (CH2Cl2/MeOH, 19:1) provided the 1-(2-trimethylsilylethoxymethyl)-benzimidazole (3.19 g, 76%) as an orange oil. 1H NMR (CDCl3) −0.05 (s, 9H), 0.90 (t, 2H, J=9 Hz), 3.51 (t, 2H, J=9 Hz), 5.55 (s, 2H), 7.32–7.37 (m, 2H), 7.55 (br d, 1H, J=6 Hz), 7.83 (br d, 1H, J=6 Hz), 7.98 (s, 1H).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07084155B2uspto-grants-2006_08