HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2263450Generated: October 26, 2026
Hexane → (2-Methoxy-3-tert-butyl-5-methylphenyl)chlorodimethylsilane
https://huagongshe.com/reaction/2263450
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Diethyldichlorosilane | HCID 15589 | — |
| Reactant | 1-Bromo-3-tert-butyl-2-methoxy-5-methylbenzene | HCID 617870 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (2-Methoxy-3-tert-butyl-5-methylphenyl)chlorodimethylsilane | HCID 11032947 | — |
Reaction Steps
Under nitrogen atmosphere, 2-methoxy-1-bromo-3-tert-butyl-5-methylbenzene (20.00 g, 77.77 mmol) was dissolved in 200 mL of diethyl ether. A 1.57 M hexane solution of n-butyllithium (59.44 mL, 93.32 mmol) was dropwise added at −50° C. or lower, and a temperature was raised to room temperature, followed by stirring for 1 hour. All the amount of diethyldichlorosilane (24.44 g, 155.54 mmol) was added to the mixture at once at −50° C. or lower, and a temperature was gradually raised to room temperature. After being refluxed for 1 hour, the solution was concentrated under reduced pressure. Hexane was added, the insolubles were filtered off with a Celite filter, and the filtrate was concentrated under reduced pressure. Concentration was further continued at 70° C. under reduced pressure for 3 hours to obtain (2-methoxy-3-tert-butyl-5-methylphenyl)chlorodimethylsilane. Resultant (2-methoxy-3-tert-butyl-5-methylphenyl)chlorodimethylsilane was used in a subsequent reaction without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07851569B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-46884fa744ed402e90d94afd22542e10 |
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| Source note | uspto-grants-2010_12 |
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