HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-(Trifluoromethoxy)benzaldehyde → 4-(TRIFLUOROMETHOXY)CINNAMIC ALDEHYDE
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-(Trifluoromethoxy)benzaldehyde | HCID 69573 | — |
| Reactant | (Triphenylphosphoranylidene)acetaldehyde | HCID 75051 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-(TRIFLUOROMETHOXY)CINNAMIC ALDEHYDE | HCID 10751191 | 60% |
Reaction Steps
570 mg (3.0 mmol) of 4-(trifluoromethoxy)benzaldehyde and 913 mg (3.0 mmol) of (triphenylphosphoranylidene)acetaldehyde were heated under reflux in 7.5 ml of toluene under nitrogen atmosphere for 1 hour and 45 minutes. The toluene was distilled off under reduced pressure and the thus obtained residue was purified over column chromatography using 20 g of silica gel. The fractions eluted with a mixed solvent of acetic acid-hexane (1:10) were collected to obtain 387 mg (yield: 60%) of the title compound as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06300357B1 |
| Source dataset | uspto-grants-2001_10 |
| ORD ID | ord-724ef7569d8948ac816bd93a5ea8b8c6 |
| Source note | uspto-grants-2001_10 |