Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Bromopropane | HCID 6358 | — |
| Reactant | Pentafluorobenzene | HCID 9696 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 178505971 | HCID 178505971 | — |
Reaction Steps
Air inside a reaction vessel of the same kind as the one used in Example 13 is displaced by a nitrogen gas in a satisfactory manner. Then, 1.503 g (0.062 mole) of magnesium, 9.770 g (0.058 mole) of pentafluorobenzene, and 15 ml of diethyl ether are charged to the reaction vessel. Also, 8.169 g (0.063 mole) of isopropyl bromide is charged to the dropping funnel. Next, isopropyl bromide is dropped to the above content with stirring under a nitrogen gas flow. After the completion of the dropping, the resulting reaction solution is subject to reaction for 2 hours at 58.0° C. with stirring. Consequently, pentafluorophenyl magnesium bromide is obtained in the form of a diethyl ether solution. A reaction yield of pentafluorophenyl magnesium bromide found in the same manner as Example 13 is 84.0 percent by mole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06683218B1 |
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| Source dataset | uspto-grants-2004_01 |
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| ORD ID | ord-6e440bfa04684742a9a963bbd1c80986 |
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| Source note | uspto-grants-2004_01 |
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