HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cesium carbonate → (3S)-1-[4-chloro-2-(trifluoromethyl)phenyl]pyrrolidin-3-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 2-Bromo-5-chlorobenzotrifluoride | HCID 136172 | — |
| Reactant | Binap, (A+-)- | HCID 634876 | — |
| Reactant | (3S)-pyrrolidin-3-ol | HCID 2733874 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | (3S)-1-[4-chloro-2-(trifluoromethyl)phenyl]pyrrolidin-3-ol | HCID 67022292 | 81.3% |
Reaction Steps
A solution of 1-bromo-4-chloro-2-(trifluoromethyl)benzene (15.0 g), (3S)-pyrrolidin-3-ol (5.0 g), palladium(II) acetate (561 mg), (±)-2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (3.11 g) and cesium carbonate (37.8 g) in toluene (280 ml) was stirred under an argon gas atmosphere at 100° C. for 18 hr. After cooling to room temperature, water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, and filtered. The filtrate was concentrated, and the residue was purified by silica gel column chromatography (hexane/ethyl acetate 95:5-80:20) to give the title compound (12.4 g, yield 81%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08338622B2 |
| Source dataset | uspto-grants-2012_12 |
| ORD ID | ord-ace196af8f554a648528af1e8bc49f79 |
| Source note | uspto-grants-2012_12 |