HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → [3,5-Bis(trifluoromethyl)benzyl](2-bromo-5-fluorobenzyl)amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Bromo-2-(bromomethyl)-4-fluorobenzene | HCID 517972 | — |
| Reactant | 3,5-Bis(trifluoromethyl)benzylamine | HCID 521099 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | [3,5-Bis(trifluoromethyl)benzyl](2-bromo-5-fluorobenzyl)amine | HCID 86615390 | — |
Reaction Steps
To a solution of 2-bromo-5-fluoro benzyl bromide (0.5 g, 1.86 mmol) and 3,5-bis(trifluoromethyl)benzylamine (0.45 g, 1.86 mmol) in methylene chloride (10 ml) at 0° C., triethyl amine (0.39 ml, 2.80 mmol) was added. The solution was slowly warmed to room temperature and stirred for 18 h. The solvent was removed under reduced pressure. The title compound was obtained by flash column chromatography using EtOAc/hexane (2:8) as the eluant. 1H NMR (CDCl3, 500 MHz) δ 7.88 (s, 2H), 7.80 (s, 1H), 7.53 (dd, J=8.8, 5.3 Hz, 1H), 7.18 (dd, J=9, 3.3 Hz, 111), 6.91 (dt, J=8.5, 3.3 Hz, 1H), 3.98 (s, 2H), 3.90 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08193365B2 |
| Source dataset | uspto-grants-2012_06 |
| ORD ID | ord-33b737d085ec4e4faf39ea0ced13adea |
| Source note | uspto-grants-2012_06 |