HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Dichloroethane → N-{4-[3,5-bis(Trifluoromethyl)pyrazol-1-yl]phenyl}cyclohexanecarboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Cyclohexanecarboxylic acid | HCID 7413 | — |
| Reactant | 2-Dimethylaminopyridine | HCID 21885 | — |
| Reactant | 4-(3,5-Bis(trifluoromethyl)-1H-pyrazol-1-yl)aniline | HCID 2740668 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-{4-[3,5-bis(Trifluoromethyl)pyrazol-1-yl]phenyl}cyclohexanecarboxamide | HCID 10158140 | — |
Reaction Steps
A mixture of cyclohexanecarboxylic acid (0.10 g, 0.8 mmol) and EDC (0.077 g, 0.4 mmol) in CH2Cl2 (1.5 mL) was stirred for 15 minutes. 1(4′-Aminophenyl)-3,5-bis(trifluoromethyl)pyrazole (0.059 g, 0.2 mmol) was added followed by dimethylaminopyridine (0.01 g, 0.1 mmol). After 3 hours the mixture was diluted with CH2Cl2 (50 mL), washed with 10% NaHCO3 (2×50 mL), brine (3×25mL), and dried over anhydrous Na2SO4. Evaporation of the solvent gave the above-named compound as a solid that crystallized from benzene (0.075 g, 92%): mp 178-180° C.; 1H NMR (CDCl3) δ 1.35 (3H, m), 1.66 (2H, m), 1.75 (1H, m), 1.85 (2H, m), 2.0 (2H, m), 2.3 (1H, m), 7.08 (1H, s), 7.45 (1H, d, J=8.5 Hz), 7.75 (2H, d, J=8.5 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06506747B1 |
| Source dataset | uspto-grants-2003_01 |
| ORD ID | ord-4ad2f92fc19141c88a5b7543995421ed |
| Source note | uspto-grants-2003_01 |