HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → N-[4-(2-chloro-ethyl)-2-methyl-phenyl]-N-methyl-acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | N-[4-(2-Chloro-ethyl)-2-methyl-phenyl]-acetamide | HCID 21963464 | — |
| Product | N-[4-(2-chloro-ethyl)-2-methyl-phenyl]-N-methyl-acetamide | HCID 21963208 | 100% |
Reaction Steps
N-[4-(2-Chloro-ethyl)-2-methyl-phenyl]-N-methyl-acetamide was prepared according to the general method as outlined in Preparation 43 starting from N-[4-(2-chloro-ethyl)-2-methyl-phenyl]-acetamide (0.450 g, 2.126 mmol) and iodomethane (0.176 ml, 2.834 mmol). After chromatographic purification, the product was isolated as a viscous oil (0.480 g, 2.125 mmol). Yield=100%. MS (APCI): 226 [M+H]+; 1H NMR (400 MHz, CDCl3) δ 7.13(bs, 1H), 7.08 (bd, J=7.57 Hz, 1H), 7.05 (d, J=7.57 Hz, 1H), 3.71 (t, J=7.06 Hz, 1H), 3.15 (s, 3H), 3.04 (t, J=7.06 Hz, 2H), 2.20 (s, 3H), 1.75 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07101886B2 |
| Source dataset | uspto-grants-2006_09 |
| ORD ID | ord-33ece3b554474c1fbe756396eb8561c6 |
| Source note | uspto-grants-2006_09 |