HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → (R)-1-(2-nitro-4-(trifluoromethyl)phenyl)piperidin-3-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 4-Fluoro-3-nitrobenzotrifluoride | HCID 67778 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | (3R)-piperidin-3-ol hydrochloride | HCID 2759333 | — |
| Solvent | Water | HCID 962 | — |
| Product | (R)-1-(2-nitro-4-(trifluoromethyl)phenyl)piperidin-3-ol | HCID 7449941 | — |
Reaction Steps
To a 100-mL round bottom flask (RBF) was added (R)-piperidin-3-ol hydrochloride (1.29 g, 9.37 mmol), sodium bicarbonate (2.76 g, 32.8 mmol), THF and 1-fluoro-2-nitro-4-(trifluoromethyl)benzene (1.31 ml, 9.37 mmol). The yellow mixture was heated to 75° C. with a water-cooled reflux condensor and allowed to stir 14 h. The reaction was filtered through a glass frit, rinsing with EtOAc, and concentrated in vacuo to give (R)-1-(2-nitro-4-(trifluoromethyl)phenyl)piperidin-3-ol as an orange oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07776869B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-c047b71878924b28a2ec04fb2c089cad |
| Source note | uspto-grants-2010_08 |