HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclopropylamine → N-cyclopropyl-N-(3-fluoro-5-nitrobenzyl)amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclopropylamine | HCID 69828 | — |
| Reactant | 1-(Bromomethyl)-3-fluoro-5-nitrobenzene | HCID 64770545 | — |
| Product | N-cyclopropyl-N-(3-fluoro-5-nitrobenzyl)amine | HCID 66906387 | 89% |
Reaction Steps
Using an analogous procedure to that described in the third paragraph of the portion of Example 12 above that is concerned with the preparation of starting materials, 3-fluoro-5-nitrobenzyl bromide was reacted with cyclopropylamine to give N-cyclopropyl N-(3-fluoro-5-nitrobenzyl)amine in 89% yield; 1H NMR: (DMSOd6) 0.25 (m, 2H), 0.35 (m, 2H), 2.03 (m, 1H), 3.02 (br s, 1H), 3.85 (s, 2H), 7.69 (m, 1H), 7.95 (m, 1H), 8.08 (s, 1H); Mass Spectrum: M+H+: 211.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08153643B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-01bbfad77b1446378314621002c6b0a2 |
| Source note | uspto-grants-2012_04 |