Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | Lithium hydride | HCID 62714 | — |
| Reactant | 1-Bromo-3,5-dimethoxybenzene | HCID 639187 | — |
| Reactant | Tris(propan-2-yl)silanethiol | HCID 3435097 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67324768 | HCID 67324768 | — |
Reaction Steps
To a solution of triisopropylsilanethiol (0.49 g, 2.6 mmol) in 1,4-dioxane (5 mL, 60 mmol) was added lithium hydride (23 mg, 2.9 mmol). After 10 minutes, 1-bromo-3,5-dimethoxy-benzene (500 mg, 2 mmol) and tetrakis(triphenylphosphine)palladium(0) (270 mg, 0.23 mmol) were added and the reaction mixture was heated to 60° C. for 16 h. The reaction mixture was diluted with DCM, filtered and concentrated. The resulting residue was dissolved in DCM and purified using silica gel chromatographie (40 g silica gel column) eluting with hexanes:DCM (3:1) to afford the title product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08765779B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-87878244df3f483ba04bced7870a61e9 |
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| Source note | uspto-grants-2014_07 |
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