HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 11404888, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 5-(Trifluoromethyl)-m-anisidine | HCID 605671 | — |
| Reactant | Diphenyl N-Cyanocarbonimidate | HCID 688090 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 11404888 | HCID 11404888 | 12.3% |
Reaction Steps
To a solution of 3-methyloxy-5-trifluoromethylaniline (11 mmol, 2.10 g) in dichloromethane (25 ml), diphenylcyanocarbonimidate (10 mmol, 2.38 g) and triethylamine (11 mmol, 1.53 ml) were added. The reaction mixture was stirred under nitrogen for 16 h at room temperature. After concentration the residue was stirred with water, the water was decanted followed by concentration. The residue was purified by flash chromatography (ethyl acetate/heptane 1:2) to give 0.413 g of the title compound (12%); Mp 168.5-169.5° C.; 1H-NMR (CDCl3): δ 3.83 (s, 3H), 7.00 (s, 1H), 7.14 (m, 3H), 7,23 (s, 1H), 7.32 (t, 1H), 7.43 ppm (t, 2H), 8.7 (br s, 1H). EI SP/MS: 335 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06147098 |
| Source dataset | uspto-grants-2000_11 |
| ORD ID | ord-ca26e8c4e0bf4756899e8dfaa4d04b4f |
| Source note | uspto-grants-2000_11 |