HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Bromo-3-chloropropane → 2-phenyl-6,7-dihydro-5H-pyrazolo[5,1-b][1,3]oxazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Bromo-3-chloropropane | HCID 8006 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 178515566 | HCID 178515566 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-phenyl-6,7-dihydro-5H-pyrazolo[5,1-b][1,3]oxazine | HCID 89488354 | — |
Reaction Steps
A mixture of 3-phenyl-1H-pyrazol-5-ol (8.80 g, 0.055 mol), 1-bromo-3-chloropropane (9.5 g, 1.1 eq, 0.06 mol) and potassium carbonate (30.3 g, 4 eq, 0.22 mol) in acetonitrile (120 mL) is heated for 5.5 h under reflux. Thereafter the volatiles are evaporated and the residue is treated with 50 mL ethyl acetate. The residual solid is washed 2× with ethyl acetate and the combined organic phases are evaporated. The obtained crude product is triturated with methyl tert butylether and 6.4 g (53%) of 2-phenyl-6,7-dihydro-5H-pyrazolo[5,1-b][1,3]oxazine are obtained as solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09023844B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-873d61d9d8ff453e991563b29e13958c |
| Source note | uspto-grants-2015_05 |