HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylamine → 6-Chloro-N-ethyl-5-nitro-2-(trifluoromethyl)pyrimidin-4-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylamine | HCID 6341 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4,6-Dichloro-5-nitro-2-(trifluoromethyl)pyrimidine | HCID 21400869 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 6-Chloro-N-ethyl-5-nitro-2-(trifluoromethyl)pyrimidin-4-amine | HCID 21400891 | 97.9% |
Reaction Steps
5.25 g (0.02 mol) of 4,6-dichloro-5-nitro-2-trifluoromethyl-pyrimidine are dissolved in 100 ml of abs. ethanol and the solution is cooled to -30° C. At this temperature, 2.0 g (0.02 mol) of triethylamine and 0.9 g (0.2 mol) of ethylamine are added. The mixture is stirred first for 4 hours at -20° C to -30° C and then for 6 hours at 0° C. After it has been left to stand overnight at 20° C, the reaction mixture is concentrated to dryness. The residue is taken up in ether and the solution washed with water. The ethereal phase is dried and concentrated to yield 5.3 g of 4-ethylamino-6-chloro-5-nitro-2-trifluoromethyl-pyrimidine as a pale yellow oil; nD20 = 1.4985.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04055411 |
| Source dataset | uspto-grants-1977_10 |
| ORD ID | ord-4765b102e8364ef38e7e526a682abea1 |
| Source note | uspto-grants-1977_10 |