HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methylamine → (2-Bromo-6-nitrophenyl)methanamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1-Bromo-2-fluoro-3-nitrobenzene | HCID 40427446 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2-Bromo-6-nitrophenyl)methanamine | HCID 66926623 | — |
Reaction Steps
A solution of 3-bromo-2-fluoronitrobenzene (1 g) in THF (8.3 ml) is heated in the presence of N,N-diisopropylethylamine (690 μA) and of methylamine (2.54 ml) in a microwave reactor (105° C., 30 min). The reaction medium is concentrated and then taken up in ethyl acetate, and then washed with water and then with brine. The organic extracts are combined, dried over magnesium sulphate, filtered and evaporated under reduced pressure. (2-Bromo-6-nitrophenyl)methylamine (1 g) is isolated in the form of an orange solid, and is used as it is in the next stage.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08507483B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-c63e8ab86e0945a2a805375bb0fd986d |
| Source note | uspto-grants-2013_08 |