HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Bromo-3,5-di-tert-butylbenzene → 1,2-Bis(bis(3,5-di-tert-butylphenyl)phosphaneyl)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Bromo-3,5-di-tert-butylbenzene | HCID 620136 | — |
| Reactant | 1,2-Bis(dichlorophosphino)benzene | HCID 3316562 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | HCID 178441125 | HCID 178441125 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1,2-Bis(bis(3,5-di-tert-butylphenyl)phosphaneyl)benzene | HCID 56646869 | — |
Reaction Steps
3,5-Di-tert-butylbromobenzene (12.50 g, 46.43 mmol) was added dropwise to magnesium (1.70 g, 69.96 mmol) and THF (50 mL) in an argon atmosphere. After the dropwise addition, the mixture was heated under reflux for 1 hour. The reaction mixture was cooled to ambient temperature and filtered, and the thus-obtained THF solution of 3,5-di-tert-butylphenylmagnesium bromide, and 1,2-bis(dichlorophosphino)benzene (2.00 g, 7.15 mmol) were reacted as in Production Example 1. The reaction was allowed to proceed overnight at 60° C. After purification, the title compound was obtained as a white powder (4.66 g, yield 73%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08637710B2 |
| Source dataset | uspto-grants-2014_01 |
| ORD ID | ord-4b3913e785514510b517fe3b1864b195 |
| Source note | uspto-grants-2014_01 |