HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 86620459, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Cyanogen Bromide | HCID 10476 | — |
| Reactant | 4-(2-Bromo-5-fluorophenoxy)piperidine | HCID 57832757 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86620459 | HCID 86620459 | — |
Reaction Steps
To a solution of 4-(2-bromo-5-fluorophenoxy)piperidine (2.0 g, 7.30 mmol) in THF (24.3 ml) was added cyanogen bromide (0.77 g, 7.30 mmol) followed by triethylamine (1.01 ml, 7.3 mmol) at 0° C. The mixture was warmed to rt and further stirred for 1 h. Solvent was evaporated and the residue was diluted with 1N HCl (20 mL). The aqueous layer was extracted with EtOAc (3×10 mL). The combined organic fractions were washed with water (20 mL) and dried over Na2SO4. The solvent was evaporated under reduced pressure to afford the title compound as a solid which was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08063224B2 |
| Source dataset | uspto-grants-2011_11 |
| ORD ID | ord-681af696eefd4038a401d315f39a9be5 |
| Source note | uspto-grants-2011_11 |