HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 2-(4-Fluorophenyl)pyrimidine-5-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 4-Fluorobenzamidine Hydrochloride | HCID 12456160 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Product | 2-(4-Fluorophenyl)pyrimidine-5-carbaldehyde | HCID 14008472 | — |
Reaction Steps
2 g (11.45 mmol) of 4-fluorobenzamidine hydrochloride, 4.09 g (11.45 mmol) of 2-dimethylaminomethylene-1,3-bis(dimethylimmonio)propane-bis(tetrafluoroborate) and 3.86 g (34.36 mmol) of potassium tert-butylate in 70 ml of ethanol were heated under reflux for 8 h. After concentration, water and ethyl acetate were added. The organic phase was washed with a potassium hydrogensulfate solution and water, dried and evaporated. Yield: 1.87 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08304438B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-47cf127e15fa4ed292425bcae8ddc936 |
| Source note | uspto-grants-2012_11 |