HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 1-Isopropenyl-4-(2,2,2-trifluoro-1,1-dimethylethyl)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Potassium (prop-1-en-2-yl)trifluoroborate | HCID 23670158 | — |
| Reactant | 4-(2,2,2-Trifluoro-1,1-dimethylethyl)Phenyl trifluoromethanesulfonate | HCID 86639046 | — |
| Catalyst | HCID 178418807 | HCID 178418807 | — |
| Solvent | 1-Propanol | HCID 1031 | — |
| Product | 1-Isopropenyl-4-(2,2,2-trifluoro-1,1-dimethylethyl)benzene | HCID 67047424 | 70% |
Reaction Steps
The procedure described in Example 10B was followed using a mixture of 4-(2,2,2-trifluoro-1,1-dimethylethyl)phenyl trifluoromethanesulfonate (13.3 g, 40 mmol), potassium isopropenyltrifluoroborate (7.0 g, 47.6 mmol), PdCl2(dppf)-CH2Cl2 (1.6 g, 1.98 mmol) and triethylamine (5.5 ml, 40 mmol) in n-propanol (400 ml). The crude residue was applied to a silica gel chromatography column and eluted with a volume mixture of hexane and EtOAc (100/1) to afford 6.32 g (70% yield) of the title compound as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07915448B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-366c5d09393b41aebd665ffc69fddde7 |
| Source note | uspto-grants-2011_03 |