HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 6-Dicyanomethyl-1,3-dimethyluracil
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Malononitrile | HCID 8010 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 6-Chloro-1,3-dimethyl-2,4(1H,3H)-pyrimidinedione | HCID 81442 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-Dicyanomethyl-1,3-dimethyluracil | HCID 13684764 | 63.2% |
Reaction Steps
Then, to a solution comprising of 100 ml of a tetrahydrofuran and 6.6 g (0.1 mole) of malononitrile was added 4.0 g (0.1 mole) of 60 wt% sodium hydride in nujol (paraffin oil) under ice-cooling, and, after adding thereto 17 g (0.1 mole) of 6-chloro-1,3-dimethyluracil, the mixture was stirred for 5 hours at room temperature. The reaction mixture thus obtained was mixed with 100 ml of water, neutralized with concentrated hydrochloric acid, and thereafter extracted with 200 ml of ethyl acetate. The extract was dried by anhydrous sodium sulfate, the solvent was distilled off under reduced pressure, and the crystals thus precipitated were collected by filtration to provide 12.9 g (63%) of 6-dicyanomethyl-1,3-dimethyluracil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04659651 |
| Source dataset | uspto-grants-1987_04 |
| ORD ID | ord-28b45f4e492846c1822da21365f68ddc |
| Source note | uspto-grants-1987_04 |