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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-(tert-Butyl-diphenyl-silanyloxy)-1-(4-chloro-phenyl)-butan-1-ol | HCID 59568826 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | tert-Butyl-[4-(4-chloro-phenyl)-4-methoxy-butoxy]-diphenyl-silane | HCID 59568823 | 100.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08119692B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-53a9dc3559c54d7c81f5529a4653033c |
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| Source note | uspto-grants-2012_02 |
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