HuagongsheHuagongshe Chemistry Print Report · For research reference only
Homoallyl bromide → 1-(3-Butenyl)-5-bromopyrimid-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Homoallyl bromide | HCID 21241 | — |
| Reactant | 5-Bromo-2(1H)-pyrimidinone | HCID 101494 | — |
| Reactant | Potassium | HCID 5462222 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-(3-Butenyl)-5-bromopyrimid-2-one | HCID 20494296 | 50% |
Reaction Steps
A mixture of the potassium salt of 5-bromopyrimid-2-one (0.01 mol) and 4-bromo-1-butene (0.015 mol) was heated in methanol (60 ml) at 70° C. for 40 h. The reaction mixture was then evaporated and the mixture extracted with chloroform. This solution was washed with 1 N NaOH (5 ml). with water (5 ml) and dried (MgSO4) before evaporating; yield 50%, m.p. 127°-128° C. (acetone). (Found: C, 42.06; H, 3.94. Calc. for C8H9BrN2O: C, 41.94; H, 3.96).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04395406 |
| Source dataset | uspto-grants-1983_07 |
| ORD ID | ord-c827da2bd0484d6e871f7e697a2c3aef |
| Source note | uspto-grants-1983_07 |