HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 7-(3-Fluorophenyl)-1-(4-methyl-1-piperazinyl)-naphthalene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Bromo-3-fluorobenzene | HCID 14082 | — |
| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | 7-Trimethylstannyl-1-(4-methyl-1-piperazinyl)-naphthalene | HCID 22115608 | — |
| Catalyst | Dichlorobis(triphenylphosphine)palladium | HCID 6102075 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Diethylether hexane | HCID 21584099 | — |
| Product | 7-(3-Fluorophenyl)-1-(4-methyl-1-piperazinyl)-naphthalene | HCID 18967542 | — |
Reaction Steps
The title product was prepared following the procedure of example 41 from 7-trimethylstannyl-1-(4-methyl-1-piperazinyl)-naphthalene (0.25 g, 0.67 mmol), 3-fluoro-1-bromobenzene (0.13 g, 0.74 mmol), triethylamine (0.45 mL, 3.23 mmol), lithium chloride (0.088 g, 2.07 mmol), and bis (triphenylphosphine) palladium chloride (0.025 g, 0.036 mmol) in DMF (12.5 mL) with a heating time of 2 hours at 120 to 130° C. The product obtained was 0.13 g (59%) in yield. A sample was obtained by recrystallization from ether/hexane for analysis: mp 116°-116.5° C. Analysis calculated for C22H21FN2 : C, 79.49; H, 6.37; N, 8.43. Found: C, 79.07; H, 6.46; N, 8.66.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05597826 |
| Source dataset | uspto-grants-1997_01 |
| ORD ID | ord-c707fa5df8a24a12a7bf570765c2d09d |
| Source note | uspto-grants-1997_01 |