HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Iodoaniline → HCID 25159658, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Iodoaniline | HCID 11995 | — |
| Reactant | 1-Ethenyl-4-ethynylbenzene | HCID 10942441 | — |
| Product | HCID 25159658 | HCID 25159658 | 72% |
Reaction Steps
The general procedure was used to convert 1-Ethynyl-4-vinyl-benzene and 2-iodoaniline to the title product. Purification by flash chromatography gave the analytically pure product as a white solid, 72% yield. 1H NMR (300 MHz, CDCl3) δ 8.31 (s, br, 1H), 7.64-7.61 (d, J=8.29, 3H), 7.49-7.46 (d, J=8.29, 2H), 7.40-7.38 (d, J=8.10, 1H), 7.22-7.16 (dt, J=6.97, 1H), 7.14-7.09 (dt, J=7.91, 1H), 6.84 (s, 1H), 6.78-6.69 (dd, J=10.73, 1H), 5.82-5.76 (dd, J=17.70, 1H), 5.30-5.26 (dd, J=10.73, 1H). Anal. Calcd. for C16H13N: C, 87.64; H, 5.98; N, 6.39.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07473786B1 |
| Source dataset | uspto-grants-2009_01 |
| ORD ID | ord-92bad07d88994efd953bbe8cf9598db9 |
| Source note | uspto-grants-2009_01 |