HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Allyl-2,2,2-trifluoroacetamide → HCID 86628469, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Allyl-2,2,2-trifluoroacetamide | HCID 558569 | — |
| Reactant | HCID 66629554 | HCID 66629554 | — |
| Product | HCID 86628469 | HCID 86628469 | — |
Reaction Steps
4-((3-bromophenyl)ethynyl)heptan-4-ol was coupled with N-allyl-2,2,2-trifluoroacetamide following the procedure described in Example 123 to give (E)-2,2,2-trifluoro-N-(3-(3-(3-hydroxy-3-propylhex-1-ynyl)phenyl)allyl)acetamide as a pale yellow oil. Yield (0.082 g, 10%): 1H NMR (400 MHz, DMSO-d6) δ 9.68 (t, J=5.4 Hz, 1H), 7.42-7.39 (m, 2H), 7.30 (t, J=8.0 Hz, 1H), 7.23 (dt, J=7.6, 1.4 Hz, 1H), 6.51 (d, J=16.0 Hz, 1H), 6.29 (dt, J=16.0, 6.0 Hz, 1H), 5.13 (s, 1H), 3.95 (t, J=5.4 Hz, 2H), 1.60-1.40 (m, 8H), 0.89 (t, J=7.2 Hz, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08492589B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-2431a571e3cd4699ad12da6fcb0a5079 |
| Source note | uspto-grants-2013_07 |