HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-Chloropyridine-3-carbaldehyde → HCID 117778379, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-Chloropyridine-3-carbaldehyde | HCID 2764053 | — |
| Reactant | Phosphonium, triphenyl[[4-(trifluoromethyl)phenyl]methyl]-, bromide | HCID 10391293 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 117778379 | HCID 117778379 | 25% |
Reaction Steps
Triphenyl[4-(trifluoromethyl)benzyl]phosphonium bromide (6.4 g) and 6-chloropyridine-3-carboxaldehyde (1.8 g) were dissolved in ethanol (120 mL). To the solution, sodium tert-butoxide (1.2 g) was added at room temperature, and the mixture was stirred for 1 hour. The solvent was distilled off under reduced pressure, and ethyl acetate was added to the residue. The organic layer was washed with water and dried over sodium sulfate. The solvent was distilled off under reduced pressure, and the obtained residue was purified by silica gel column chromatography (Yamazen Corporation, elution solvent: hexane/ethyl acetate). The obtained solid was washed with hexane to obtain the title compound (0.89 g) (yield: 25%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09212170B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-00bab5032f7e4777b4b330a604dd6db0 |
| Source note | uspto-grants-2015_12 |