HuagongsheHuagongshe Chemistry Print Report · For research reference only
Gallium, chlorodimethyl- → o-Trifluoromethylbenzyldimethylgallium
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Gallium, chlorodimethyl- | HCID 81329 | — |
| Reactant | 1-(Bromomethyl)-2-(trifluoromethyl)benzene | HCID 123057 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Hexane | HCID 8058 | — |
| Solvent | Diethylether hexane | HCID 21584099 | — |
| Product | o-Trifluoromethylbenzyldimethylgallium | HCID 14692906 | — |
Reaction Steps
5.25 g (22 mmol) of o-trifluoromethylbenzyl bromide in 10 ml of ether/hexane are added at -50° to a mixture of 45 ml of ether/hexane (2:1) and 14.7 ml (1.5N =22 mmol) of n-butyllithium. After stirring for 15 minutes, 2.1 g (16 mmol) of dimethylgallium chloride in 20 ml of hexane are added. Then the reaction mixture is allowed to come to room temperature, it is stirred for 24 hours, and the LiCl is filtered off and the solvent removed. After sublimation in vacuo, o-trifluoromethylbenzyldimethylgallium is obtained with a Mp. 35°-38°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05099044 |
| Source dataset | uspto-grants-1992_03 |
| ORD ID | ord-7db2b241997c47a39394763b74c9d79f |
| Source note | uspto-grants-1992_03 |