HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Allyl-2,2,2-trifluoroacetamide → HCID 86635870, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Allyl-2,2,2-trifluoroacetamide | HCID 558569 | — |
| Reactant | HCID 914041 | HCID 914041 | — |
| Product | HCID 86635870 | HCID 86635870 | — |
Reaction Steps
Heck coupling of N-(3-bromobenzyl)cyclohexanamine and N-allyl-2,2,2-trifluoroacetamide following the method described in Example 118 gave (E)-N-(3-(3-((cyclohexylamino)methyl)phenyl)allyl)-2,2,2-trifluoroacetamide as a colorless oil. Yield (0.20 g, 22%): 1H NMR (400 MHz, CD3OD) δ 7.55 (s, 1H), 7.48-7.50 (m, 1H), 7.42 (t, J=7.6 Hz, 1H), 7.35-7.37 (m, 1H), 6.61 (d, J=16.0 Hz, 1H), 6.32 (dt, J=16.0, 6.4 Hz, 1H), 4.19 (s, 2H), 4.05 (d, J=6.4 Hz, 2H), 3.07-3.16 (m, 1H), 2.14-2.22 (m, 2H), 1.66-1.82 (m, 2H), 1.68-1.76 (m, 1H), 1.16-1.50 (m, 5H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08716529B2 |
| Source dataset | uspto-grants-2014_05 |
| ORD ID | ord-d9d42c54d764471daf04baa5eb29d4f8 |
| Source note | uspto-grants-2014_05 |