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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 460372Generated: October 29, 2026

Imidazole → 4-(t-Butyldimethylsiloxy)methyl-1-t-butyldiphenylsiloxy-3,5-dimethoxybenzene

https://huagongshe.com/reaction/460372

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantWaterHCID 962—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
ReactantHCID 69363687HCID 69363687—
SolventDimethylformamideHCID 6228—
Product4-(t-Butyldimethylsiloxy)methyl-1-t-butyldiphenylsiloxy-3,5-dimethoxybenzeneHCID 69364307—

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of the crude 4-t-butyldiphenylsiloxy-2,6-dimethoxybenzyl alcohol (4.01 g) obtained by the above-described procedure in anhydrous dimethylformamide (30 mL) were added imidazole (1.29 g, 18.98 mmol) and t-butylchlorodimethylsilane (1.79 g, 11.86 mmol). After stirring at 50° C. for 4 hours, water was added and the resulting mixture was extracted with ethyl acetate-hexane (1:2). The organic layer was washed with water, dried over anhydrous sodium sulfate, and concentrated under reduced pressure to yield crude 4-(t-butyldimethylsiloxy)methyl-1-t-butyldiphenylsiloxy-3,5-dimethoxybenzene was obtained as a colorless amorphous powder (5.33 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07196101B2
Source datasetuspto-grants-2007_03
ORD IDord-fa12ba6fd76b42b8b0b5976d6d45e0bb
Source noteuspto-grants-2007_03