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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1601124Generated: October 30, 2026

Imidazole → HCID 21831156, compound

https://huagongshe.com/reaction/1601124

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantDimethylformamideHCID 6228—
ReactantMandelonitrileHCID 10758—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
ProductHCID 21831156HCID 2183115682%

Reaction Conditions

Temperature35 °C

Reaction Steps

Mandelonitrile (50 g, 0.38 moles) and imidazole (64 g, 0.94 moles) were dissolved in DMF (100 cm3) and the resulting solution cooled in an ice-water bath. tert-Butyldimethylsilyl chloride (68 g, 0.45 moles) was then added portionwise over a period of 20 minutes. The flask contents were then warmed to 35° C. and stirred at that temperature for 18 hours. The reaction mixture was then cooled and partitioned between ethyl acetate (3×100 cm3) and deionised water (100 cm3). The combined organic fractions were then washed with brine (100 cm3), dried over anhydrous magnesium sulphate and concentrated under reduced pressure to give the crude product as a yellow oil. Flash chromatography (600 g kieselgel 60 silica) eluting with 20% dichloromethane in pentane gave the title compound as an oil (77 g, 0.31 moles, 82%), δH (300 MHz;CDCl3) 0.1 (3H, s), 0.2 (3H, s), 1.0 (9H, s), 5.5 (1H, s), and 7.4 (5H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05977142
Source datasetuspto-grants-1999_11
ORD IDord-0d9c1e657bf84af785357edbb1c3ae72
Source noteuspto-grants-1999_11