HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butyl methyl ether → 4-Bromo-1-fluoro-2-fluoromethyl-3-butyn-2-yl 4-Trifluoromethylphenyl Ether
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butyl methyl ether | HCID 15413 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 1-Fluoro-2-fluoromethyl-3-butyn-2-yl 4-trifluoromethylphenyl ether | HCID 18424404 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 4-Bromo-1-fluoro-2-fluoromethyl-3-butyn-2-yl 4-Trifluoromethylphenyl Ether | HCID 18424415 | — |
Reaction Steps
An amount (13.9 g) of 1-fluoro-2-fluoromethyl-3-butyn-2-yl 4-trifluoromethylphenyl ether was dissolved in a solvent consisting of a mixture of tert-butyl methyl ether (100 ml) and tert-butyl alcohol (150 ml). To the solution under cooling with ice, potassium tert-butoxide (7.1 g) was added under a nitrogen atmosphere; after stirring for a while, bromine (3 ml) was added dropwise. After the end of the dropwise addition, the mixture was stirred for 30 minutes under stirring with ice. Hexane was added to the reaction mixture, which was then washed with water and a saturated aqueous solution of sodium chloride. The mixture was dried with anhydrous sodium sulfate and concentrated under reduced pressure to give the titled compound (18.1 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06455708B1 |
| Source dataset | uspto-grants-2002_09 |
| ORD ID | ord-81847dd3e14447bd8eb9f9c76f73b72c |
| Source note | uspto-grants-2002_09 |