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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2252392Generated: November 2, 2026

Imidazole → 4-(Tert-butyldimethylsilyloxy)-phenyl-acetonitrile

https://huagongshe.com/reaction/2252392

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactant4-Hydroxybenzyl cyanideHCID 26548—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
Product4-(Tert-butyldimethylsilyloxy)-phenyl-acetonitrileHCID 1833358298%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of 4-hydroxybenzyl cyanide 77 (2.0 g, 15.0 mmol) in DMF (10 ml) was added t-butyldimethylsilyl chloride (2.5 g, 16.5 mmol). The reaction mixture was cooled to 0° C. and imidazole (2.3 g, 33.0 mmol) was added and then the mixture was allowed to warm to ambient temperature. After stirring for 3 hours, the reaction mixture was diluted with ether and washed with 0.5 M HCl, sat. aq. NaHCO3, water, and brine, then dried over MgSO4. The crude product was purified via flash SiO2 (eluted with hexane/ethyl acetate (8:1)) to give 78 as a clear oil (3.6 g, 98% yield). 1H-NMR (400 MHz, chloroform-d) δ7.87 (d, J=8.5 Hz, 2 H), 6.86 (d, J=8.5 Hz, 2 H), 3.54 (s, 2 H), 0.98 (s, 9 H), 0.23 (s, 6 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07321065B2
Source datasetuspto-grants-2008_01
ORD IDord-ca613ec388ab4b058488aa1c994e123e
Source noteuspto-grants-2008_01