HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetoacetate → 3-Allyl-6-methyluracil
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetoacetate | HCID 8868 | — |
| Reactant | Allylurea | HCID 11181 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Catalyst | Hydrochloric Acid | HCID 313 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-Allyl-6-methyluracil | HCID 13602047 | — |
Reaction Steps
To allylurea (25 g, 25 mol) in ethanol (10 mL) was added ethyl acetoacetate (31.86 mL, 25 mol) and 10 drops conc. HCl. After 12 days at room temperature, concentration gave an oil which was dissolved in MeOH. KOH (22.5 g, 0.34 mol) was added and the solution refluxed for 1 hour. After neutralization, the resulting solid 1 was collected. Yield 2.7 g (7%). NMR (CDCl3) δ: 2.16 (3H, s), 4.52 (2H, d), 5.18 (1H, d), 5.23 (1H, d), 5.60 (1H, s), 5.82-5.93 (1H, m), 10.3 (1H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06872728B2 |
| Source dataset | uspto-grants-2005_03 |
| ORD ID | ord-37a753e57f2a4877acb3d87e58643f7f |
| Source note | uspto-grants-2005_03 |