HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Bromide → (3-Ethoxy-5,6-difluoronaphthalen-2-yl)trimethylsilane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Bromide | HCID 6332 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 7,8-Difluoro-3-trimethylsilanylnaphthalen-2-ol | HCID 58151937 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | (3-Ethoxy-5,6-difluoronaphthalen-2-yl)trimethylsilane | HCID 58151894 | — |
Reaction Steps
54.7 g (about 0.12 mol) of 7,8-difluoro-3-trimethylsilanylnaphthalen-2-ol are stirred at 80° C. for 19 h together with 19.5 ml (0.26 mol) of bromoethane and 34.5 g (0.25 mol) of potassium carbonate in 400 ml of ethyl methyl ketone. The batch is filtered, and the residue is washed with ethyl methyl ketone. The filtrate is concentrated, and the residue is taken up in MTBE. The solution is washed with water and sat. sodium chloride soln. and dried using sodium sulfate. The residue remaining after removal of the solvent is purified by column chromatography (SiO2, toluene:ethyl acetate=9:1), giving (3-ethoxy-5,6-difluoronaphthalen-2-yl)trimethylsilane as a dark-brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08303844B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-156dac9c313249acadc8205f37becccb |
| Source note | uspto-grants-2012_11 |