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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2083521Generated: October 28, 2026

Imidazole → {[1-(4-Fluorophenoxy)but-3-yn-2-yl]oxy}(trimethyl)silane

https://huagongshe.com/reaction/2083521

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantChlorotrimethylsilaneHCID 6397—
Reactant1-(4-Fluorophenoxy)but-3-yn-2-olHCID 12786216—
SolventHexaneHCID 8058—
Product{[1-(4-Fluorophenoxy)but-3-yn-2-yl]oxy}(trimethyl)silaneHCID 1278621791%

Reaction Steps

To a 0° C solution of 10 g (55 mmoles) of 3-hydroxy-4-p-fluorophenoxy-1-butyne (Example 157) in 75 ml of dry dimethylformamidee and 88 g (130 mmoles) of imidazole is added dropwise, with stirring, 7.5 g (68 mmoles) of chlorotrimethylsilane. The mixture, while under an argon atmosphere, is stirred at room temperature for 18 hours, and then poured into 150 ml of hexane and 100 ml of ice-water. Thhe organic phase is separated, washed with 50 ml of a brine solution, dried with magnesium sulfate, and evaporated under vacuum. This crude product is distilled under vacuum at 0.1 mm (bp 73°-75° C), to give 12.2 g (91%) of the subject compound as a colorless oily liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04085272
Source datasetuspto-grants-1978_04
ORD IDord-59aa7426e6ac48f89a234eb1d20fc1c7
Source noteuspto-grants-1978_04