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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22534Generated: October 25, 2026

Chlorotrimethylsilane → 4-(3-Formyl-n-propyl)-1-trimethylsilylimidazole

https://huagongshe.com/reaction/22534

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantSodium hydrideHCID 24758—
ReactantHCID 178471275HCID 178471275—
SolventTetrahydrofuranHCID 8028—
Product4-(3-Formyl-n-propyl)-1-trimethylsilylimidazoleHCID 19930428—

Reaction Steps

A solution of 1.82 g of 4-(3-ethoxycarbonylpropyl)-1H-imidazole in 30 ml of tetrahydrofuran under nitrogen is treated with 0.5 g of sodium hydride (50% oil dispersion ) at 0° for 30 min and 1.45 ml of trimethylsilyl chloride at 0° for 3 h. The reaction mixture is washed with cold 0.5N sodium bicarbonate solution, dried over sodium sulfate and evaporated to dryness. The oil is redissolved in 100 ml of methylene chloride at -78° under nitrogen and 12.82 ml of diisobutylaluminium hydride (1.56M) is added dropwise. The reaction mixture is stirred for 5 min at -78°, quenched with 1 ml of methanol followed by 10 ml of water and filtered through Celite®. The organic phase is separated, dried over sodium sulfate and evaporated to yield the title compound a).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05428160
Source datasetuspto-grants-1995_06
ORD IDord-a5509104bf3a4556a685852c2da07def
Source noteuspto-grants-1995_06