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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1518636Generated: November 4, 2026

Imidazole → Tert-butyldimethyl{[8-(3-nitro-4-phenylphenoxy)octyl]oxy}silane

https://huagongshe.com/reaction/1518636

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant8-(3-Nitro-4-phenylphenoxy)octan-1-olHCID 66597342—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyldimethyl{[8-(3-nitro-4-phenylphenoxy)octyl]oxy}silaneHCID 6659740286.1%

Reaction Steps

8-(3-Nitro-4-phenylphenoxy)octan-1-ol (1.23 g, 3.5 mmol) and imidazole (408 mg, 6.0 mmol) were dissolved in tetrahydrofuran (15 mL) and a solution of tert-butyldimethylchlorosilane (750 mg, 5.0 mmol) in tetrahydrofuran (5 mL) was added thereto. After stirring the reaction mixture at room temperature for 18 hours, purified water was added to stop the reaction and the mixture was extracted with ethyl acetate. The organic layer was washed with a saturated aqueous solution of sodium bicarbonate, a saturated aqueous solution of ammonium chloride, and a saturated aqueous solution of sodium chloride, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by flash column chromatography to obtain tert-butyldimethyl{[8-(3-nitro-4-phenylphenoxy)octyl]oxy}silane (1.38 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09072734B2
Source datasetuspto-grants-2015_07
ORD IDord-b99669a7b4c243d8a5ccdf71818e465a
Source noteuspto-grants-2015_07