HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Bromide → 3-ethyl-1-(4-nitrophenyl)-2,4(1H,3H)-pyrimidinedione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Bromide | HCID 6332 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 1-(4-Nitrophenyl)pyrimidine-2,4-dione | HCID 11276338 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | 3-ethyl-1-(4-nitrophenyl)-2,4(1H,3H)-pyrimidinedione | HCID 15125479 | 65.6% |
Reaction Steps
A mixture of 3 parts of 1-(4-nitrophenyl)-2,4(1H,3H)-pyrimidinedione, 1,4 parts of potassium hydroxide and 67.5 parts of N,N-dimethylacetamide was stirred for 1 hour at room temperature under nitrogen atmosphere. 1.52 Parts of bromoethane were added and stirring was continued overnight at room temperature. The reaction mixture was poured into 100 parts of ice water. The product was filtered off and stirred in methanol. The product was filtered off and dried in vacuo at 60° C., yielding 2.4 parts (65.6%) of 3-ethyl-1-(4-nitro-phenyl)-2,4(1H,3H)-pyrimidinedione; mp. 182.5° C. (int. 24).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04931444 |
| Source dataset | uspto-grants-1990_06 |
| ORD ID | ord-d072a9a384e947f2a9bfee02dda21a87 |
| Source note | uspto-grants-1990_06 |