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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 983644Generated: November 2, 2026

Benzimidazole → 1-(2-Trimethylsilylethoxymethyl)-2-formyl-benzimidazole

https://huagongshe.com/reaction/983644

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzimidazoleHCID 5798—
ReactantDimethylformamideHCID 6228—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Chloromethyl 2-(trimethylsilyl)ethyl etherHCID 2724271—
Product1-(2-Trimethylsilylethoxymethyl)-2-formyl-benzimidazoleHCID 1201712876%

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06864265B2
Source datasetuspto-grants-2005_03
ORD IDord-04f5822688c84246b094b99761f2e97a
Source noteuspto-grants-2005_03