HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Hydroxybenzaldehyde → Benzaldehyde, 3-(4-fluorophenoxy)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Hydroxybenzaldehyde | HCID 101 | — |
| Reactant | 1-Bromo-4-fluorobenzene | HCID 9993 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Catalyst | Copper | HCID 23978 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | Benzaldehyde, 3-(4-fluorophenoxy)- | HCID 3085320 | 73% |
Reaction Steps
A heterogeneous mixture of 3-hydroxybenzaldehyde (9.16 g, 75 mmol), 4-bromofluorobenzene (27.30 g, 156 mmol), K2CO3 (16.07 g, 116.3 mmol) and copper powder (2.38 g, 37.5 mmol) in pyridine (75 mL) was refluxed for 40 hrs. It was then cooled to room temperature and filtered through Celite. The filtrate was diluted with ethylacetate (500 mL) and washed with water (3×300 mL). The organic was then dried with MgSO4 and concentrated. The resulting residue was chromatographed (silica gel, hexane:ether, 85:15) to afford 11.83 g (73%) of 3-(4-fluorophenoxy)benzaldehyde as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05120752 |
| Source dataset | uspto-grants-1992_06 |
| ORD ID | ord-d691195a23ed47748117a4e2251b82c3 |
| Source note | uspto-grants-1992_06 |