Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1643307Generated: October 31, 2026

Methyl iodide → tert-Butyl-[4-(4-chloro-phenyl)-4-methoxy-butoxy]-diphenyl-silane

https://huagongshe.com/reaction/1643307

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant4-(tert-Butyl-diphenyl-silanyloxy)-1-(4-chloro-phenyl)-butan-1-olHCID 59568826—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl-[4-(4-chloro-phenyl)-4-methoxy-butoxy]-diphenyl-silaneHCID 59568823100.9%

Reaction Steps

To a suspension of NaH (153 mg 60% dispersed in mineral oil, 6.39 mmol) in 20 mL THF was slowly added at room temperature 4-(tert-butyl-diphenyl-silanyloxy)-1-(4-chloro-phenyl)-butan-1-ol (330 mg, 0.75 mmol) as a solution in 10 mL THF followed by the dropwise addition of methyl iodide (339 μL, 5.25 mmol). The reaction mixture was stirred for 3 h at room temperature before being quenched by the careful addition of saturated aqueous NH4Cl (30 mL). The mixture was extracted with ethylacetate (3×30 mL) and the combined organic layers washed with brine (2×20 mL) and dried over sodium sulfate. After evaporation of solvent the product was isolated by flash column chromatography eluting with 0% to 30% ethyl acetate/hexane to give 343 mg of the title compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119692B2
Source datasetuspto-grants-2012_02
ORD IDord-53a9dc3559c54d7c81f5529a4653033c
Source noteuspto-grants-2012_02