HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetramethoxysilane → 2-(Trimethoxysilyl)thianthrene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetramethoxysilane | HCID 12682 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | 2-Bromothianthrene | HCID 13213122 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(Trimethoxysilyl)thianthrene | HCID 71116697 | 60% |
Reaction Steps
A 3-neck 1 L flask was filled with magnesium turnings (5 g), THF (200 g) and tetramethoxysilane (50 g), and heated to reflux. 2-Bromothianthrene (40 g), prepared analogously to Example 3A was added to the flask in 10 g portions. Grignard started within 10 minutes. The reaction was allowed to cool for 1 hour, after which magnesium salts were precipitated with hexanes (200 mL). GC/MS of the solution showed that along with some thianthrene, 2-(trimethoxysilyl)thianthrene was obtained in ˜60% yield (FIG. 7).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09190616B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-c3be22e915f540efa35b32c846145ac7 |
| Source note | uspto-grants-2015_11 |