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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 628378Generated: October 26, 2026

Imidazole → (3-(((Tert-butyldiphenylsilyl)oxy)methyl)phenyl)methanol

https://huagongshe.com/reaction/628378

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactant1,3-BenzenedimethanolHCID 69374—
Reactanttert-ButyldiphenylchlorosilaneHCID 94078—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product(3-(((Tert-butyldiphenylsilyl)oxy)methyl)phenyl)methanolHCID 57049439—

Reaction Steps

To a solution of 1,3-phenylenedimethanol (10.00 g, 72.38 mmol, Aldrich) in DCM (200 mL) was added 1H-imidazole (5.17 g, 76.0 mmol, Aldrich), followed by the addition of tert-butylchlorodiphenylsilane (19.8 mL, 76.0 mmol, Aldrich) and 4-dimethylaminopyridine (0.88 g, 7.2 mmol, Aldrich). After stirring overnight, the reaction was partitioned between DCM and water, the organic layer was dried over sodium sulfate, filtered and concentrated. The product was purified by flash chromatography (gradient elution, 0 to 20% EtOAc/hexanes). Yield: (7.9 g, 29%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09309246B2
Source datasetuspto-grants-2016_04
ORD IDord-da68729bd8b14e24992ff15ebf72999b
Source noteuspto-grants-2016_04