Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1,3-Dimethoxybenzene | HCID 9025 | — |
| Reactant | Silane, chloro(chloromethyl)dimethyl- | HCID 74393 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 13392354 | HCID 13392354 | 84% |
Reaction Steps
A solution of 25.0 g (0.181 mol) of 1,3-dimethoxybenzene in 250 ml of tetrahydrofuran was stirred at room temperature under nitrogen while 125 ml (0.200 mol) of 1.6 molar n-butyllithium in hexane was added dropwise over 30 minutes. The resulting mixture was refluxed 1.5 hour, giving an orange-brown solution that was cooled to 5° and stirred while 27 ml (29.4 g, 0.205 mol) of chloro(chloromethyl)dimethylsilane was added dropwise over 15 minutes. The resulting white suspension was allowed to warm to room temperature, stirred there 1 hour, diluted with ethyl acetate, poured into water, and extracted with ether. The organic layers were washed with brine, dried over magnesium sulfate, and distilled to give 37.0 g (84%) of the title compound as a colorless liquid: bp 98°-110° (0.1 mm); nmr (CDCl3) 0.4 (6H, s), 3.1 (2H, s), 3.7 (6H, s), 6.3 (2 H, d), 7.1 (1H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04496551 |
|---|
| Source dataset | uspto-grants-1985_01 |
|---|
| ORD ID | ord-e8cff534e0a34c5f820f42bb2aff6583 |
|---|
| Source note | uspto-grants-1985_01 |
|---|