HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(Dicyclohexylphosphino)-2'-(dimethylamino)biphenyl → HCID 24937078, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(Dicyclohexylphosphino)-2'-(dimethylamino)biphenyl | HCID 2734217 | — |
| Reactant | 6-(Trifluoromethyl)-1,2,3,4-tetrahydroisoquinoline hydrochloride | HCID 21712558 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | N-(4-Bromo-2,6-dimethyl-phenyl)-3,3-dimethyl-butanamide | HCID 59741059 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 24937078 | HCID 24937078 | — |
Reaction Steps
Bis(dibenzylidineacetone)palladium (390 mg, 0.68 mmol) and (2′-dicyclohexylphosphanyl-biphenyl-2-yl)-dimethylamine (800 mg, 2.0 mmol) were added to dry toluene (150 mL purged with argon) and stirred for 15 minutes under argon. Potassium tert-butoxide (4.75 mg, 42.3 mmol), 6-Trifluoromethyl-1,2,3,4-tetrahydroisoquinoline hydrochloride salt (4.82 g, 20.3 mmol) and N-(4-Bromo-2,6-dimethyl-phenyl)-3,3-dimethyl-butyramide (5 g, 16.8 mmol) were then added and the reaction mixture was stirred at 80° C. over night. The reaction mixture was then cooled to room temperature and recrystallized from toluene to afford the title compound as a solid. (5.55 g, 79%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08993593B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-3c142aeaba6f4b77ba1c5b6168a738f5 |
| Source note | uspto-grants-2015_03 |