HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Allyl-2,2,2-trifluoroacetamide → HCID 86635871, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Allyl-2,2,2-trifluoroacetamide | HCID 558569 | — |
| Reactant | 3-bromo-N-cyclohexylbenzamide | HCID 2306322 | — |
| Product | HCID 86635871 | HCID 86635871 | — |
Reaction Steps
Heck coupling of 3-bromo-N-cyclohexylbenzamide and N-allyl-2,2,2-trifluoroacetamide following the method described in Example 118 gave (E)-N-cyclohexyl-3-(3-(2,2,2-trifluoroacetamido)prop-1-enyl)benzamide as a light yellow solid. Yield (0.50 g, 71%): 1H NMR (400 MHz, CD3OD) δ 8.18-8.26 (m, 1H), 7.83 (t, J=1.6 Hz, 1H), 7.65-7.68 (m, 1H), 7.54-7.56 (m, 1H), 7.39 (t, J=7.6 Hz, 1H), 6.62 (d, J=16.0 Hz, 1H), 6.32 (dt, J=16.0, 6.4 Hz, 1H), 4.06 (d, J=5.6 Hz, 2H), 3.80-3.90 (m, 1H), 1.93-1.95 (m, 2H), 1.79-1.82 (m, 2H), 1.66-1.70 (m, 1H), 1.18-1.48 (m, 5H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09056849B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-d629803ff4f74c44a7360043adce7ad9 |
| Source note | uspto-grants-2015_06 |