HuagongsheHuagongshe Chemistry Print Report · For research reference only
o-Iodonitrobenzene → HCID 24821367, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | o-Iodonitrobenzene | HCID 69115 | — |
| Reactant | Myristanilide | HCID 69324 | — |
| Product | HCID 24821367 | HCID 24821367 | 85% |
Reaction Steps
The title compound was prepared with the analogous procedure described in example 1 using 1-Iodo-2-nitrobenzene (125 mg, 0.5 mmol) and myristanilide (182 mg, 0.6 mmol) as starting materials to yield the title compound as colorless oil (160 mg, 85%). 1H NMR (DMSO) δ 0.74 (t, J=6.9 Hz, 3 H), 1.14-1.28 (m, 20 H), 1.68 (p, J=7.6 Hz, 2 H), 2.83 (t, J=7.6 Hz, 2 H), 7.14 (d, J=8.1 Hz, 1 H), 7.29 (dd, J=8.1, 7.7 Hz, 1 H), 7.47 (dd, J=8.1, 7.7 Hz, 1 H), 7.56-7.68 (m, 5 H), 7.74 (d, J=7.7 Hz, 1 H); 13C NMR δ 13.9, 22.0, 26.3, 26.4, 28.3, 28.4, 28.7, 28.8, 28.9, 29.9, 31.2, 110.7, 116.9, 123.5, 123.7, 127.2, 129.6, 130.1, 134.2, 135.0, 137.6, 154.7. HRMS (FAB): cal. for C26H36N2 [M+H+]: 377.2957; found: 377.2953.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08735586B2 |
| Source dataset | uspto-grants-2014_05 |
| ORD ID | ord-6bc1fef060944713ba2d4fa9f9ab3151 |
| Source note | uspto-grants-2014_05 |