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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 488120Generated: October 30, 2026

Imidazole → 1-(t-Butyldimethylsilyl)oxymethyl-4-methoxymethoxy-5-methylnaphthalene

https://huagongshe.com/reaction/488120

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant1-Hydroxymethyl-4-methoxymethoxy-5-methylnaphthaleneHCID 14986454—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventWaterHCID 962—
Product1-(t-Butyldimethylsilyl)oxymethyl-4-methoxymethoxy-5-methylnaphthaleneHCID 1498645591%

Reaction Steps

13.7 g of t-butylchlorodimethylsilane was added to an N,N-dimethylaminopyridine (100 ml) solution of 14 g of 1-hydroxymethyl-4-methoxymethoxy-5-methylnaphthalene,6.64 g of imidazole, and 0.4 g of 4-dimethylaminopyridine and agitated at room temperature overnight. Water was added to the reaction solution, followed by extraction with ethyl acetate. Thereafter, the resultant organic phase was washed with water and then with a saturated saline solution. After drying with anhydrous magnesium sulfate, the solvent was distilled off and the residue was purified by silica gel column chromatography (5% ethyl acetate/hexane) to obtain 19 g of the captioned compound as a light brown oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05298649
Source datasetuspto-grants-1994_03
ORD IDord-47477dfd1ee04e73b9e2ebf4599fe68f
Source noteuspto-grants-1994_03