HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 3-Methyl-5-(trifluoromethyl)dihydropyrimidine-2,4(1H,3H)-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Methylurea | HCID 11719 | — |
| Reactant | 2-(Trifluoromethyl)prop-2-enoyl chloride | HCID 10149016 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-Methyl-5-(trifluoromethyl)dihydropyrimidine-2,4(1H,3H)-dione | HCID 13004979 | 30% |
| Product | 1-Methyl-5-(trifluoromethyl)dihydropyrimidine-2,4(1H,3H)-dione | HCID 13004980 | 10% |
Reaction Steps
A solution of methylurea (148 mg; 2.0 mmoles) in DMF (2 ml) was cooled to 0° C., and α-trifluoromethylacryloyl chloride (317 mg; 2.0 mmoles) was added dropwise. The mixture was stirred at room temperature for 1 hour, and water (20 ml) was added. The mixture was extracted with methylene chloride (20 ml×1, 10 ml×2). The combined extracts were dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The residue was purified by a column chromatography on silica gel (chloroform:ethyl acetate=3:1) to give 39 mg (yield: 10%) of 1-methyl-5-trifluoromethyl-5,6-dihydrouracil (OF-3) and 117 mg (yield: 30%) of 3-methyl-5-trifluoromethyl-5,6-dihydrouracil (OF-2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04581452 |
| Source dataset | uspto-grants-1986_04 |
| ORD ID | ord-cbc7d333692443de91618c2cf3611781 |
| Source note | uspto-grants-1986_04 |