HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → HCID 20435498, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Carbonic acid-guanidine (1:1) | HCID 286947 | — |
| Reactant | HCID 10964906 | HCID 10964906 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 20435498 | HCID 20435498 | 59% |
Reaction Steps
A mixture of 6.0 g 3-carbethoxy-5-hexyn-2-one and 3.6 g guanidine carbonate was heated in 9 ml dimethylsulfoxide under a nitrogen atmosphere at 140° for 4 hours. The ethanol produced in the reaction was removed as it was formed by distillation. After cooling to room temperature, acetone was added then the crystalline solid was collected then rinsed with water to yield 2.6 g of 4,6-dimethylfuro[2,3-d]pyrimidine; m.p. 262°-263°. Absorptions at 2.55 (singlet), 2.82 (singlet) and 6.58 (broadened singlet) ppm in the nuclear magnetic resonance spectrum (60 MHz) indicated the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04487626 |
| Source dataset | uspto-grants-1984_12 |
| ORD ID | ord-42f19fc85ff748fb8ba3240fae187f04 |
| Source note | uspto-grants-1984_12 |