HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chlorobenzaldehyde → 4-(Pyridin-2-ylsulfanyl)benzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chlorobenzaldehyde | HCID 7726 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 178418616 | HCID 178418616 | — |
| Solvent | Hexamethylphosphoramide | HCID 12679 | — |
| Product | 4-(Pyridin-2-ylsulfanyl)benzaldehyde | HCID 13392576 | 42.2% |
Reaction Conditions
| Temperature | 140 °C |
|---|
Reaction Steps
A mixture of 18.4 g of 2-pyridinethiol, 23.2 g of 4-chlorobenzaldehyde, 40 g of potassium carbonate and 100 ml of hexamethylphosphoramide was heated at a temperature of 140° C. for 4 hours. After cooling, the mixture was filtered and the filtrate was concentrated. The resulting oily substance was dissolved in diethyl ether and the solution was washed successively with an aqueous solution of sodium hydroxide and water, and dried over magnesium sulfate. The solvent was distilled off and the resulting oily substance was distilled under reduced pressure to obtain 15 g (42% yield) of 4-(2-pyridylthio)benzaldehyde as a colorless oil having a boiling point of 136° C./2 mmHg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04496735 |
| Source dataset | uspto-grants-1985_01 |
| ORD ID | ord-764d786d4b5c475098dedf563366506b |
| Source note | uspto-grants-1985_01 |