HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → Dibenzyl-(2,4-difluoro-phenyl)-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | 2,4-Difluoroaniline | HCID 9709 | — |
| Solvent | Water | HCID 962 | — |
| Product | Dibenzyl-(2,4-difluoro-phenyl)-amine | HCID 58086650 | 90% |
Reaction Steps
To 2,4-difluoro-phenylamine (a, 2.0 g, 15.5 mmol) in N,N-dimethylformamide (20 mL) potassium carbonate (6.0 g, 45 mmol) and benzyl bromide (5.49 mL, 35 mmol) were added. The reaction was stirred at room temperature overnight. The reaction was poured into water and extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate and filtered. The filtrate was concentrated under reduced pressure and purified by silica gel column chromatography eluting with hexane to give dibenzyl-(2,4-difluoro-phenyl)-amine as colourless oil (4.34 g, 90%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08524707B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-8b88a8896a624baaa7d77a3f19871ca1 |
| Source note | uspto-grants-2013_09 |