HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetanilide → HCID 12798655, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetanilide | HCID 904 | — |
| Reactant | HCID 66720019 | HCID 66720019 | — |
| Product | HCID 12798655 | HCID 12798655 | 67% |
Reaction Steps
Method A applied to 4-dimethoxymethyl-1-iodo-2-nitrobenzene (155 mg, 0.5 mmol) and N-phenylacetamide (81 mg, 0.6 mmol) yielded the title compound as pale yellow oil (79 mg, 67% yield). 1H NMR (DMSO) δ 2.50 (s, 3H), 7.31 (d, J=8.3Hz, 1H), 7.61-7.68 (m, 5H), 7.82 (d, J=8.3Hz, 1H), 8.25 (s, 1H), 10.10 (s, 1H); 13C NMR δ 13.6, 111.4, 120.1, 124.2, 127.0, 129.8, 130.2, 132.3, 139.1, 154.7, 158.3, 192.4. HRMS (FAB): cal. for C15H13N2O [M+H+]: 237.1028; found: 237.1024.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08188282B2 |
| Source dataset | uspto-grants-2012_05 |
| ORD ID | ord-0b821fa0a0eb4530bb435656b57e1b9f |
| Source note | uspto-grants-2012_05 |