HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 4-{[(2,4,5-Trichlorophenyl)sulfanyl]carbonyl}phenyl acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 2,4,5-Trichlorobenzenethiol | HCID 19597 | — |
| Reactant | p-Acetoxybenzoyl chloride | HCID 2756254 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-{[(2,4,5-Trichlorophenyl)sulfanyl]carbonyl}phenyl acetate | HCID 71333216 | 97% |
Reaction Steps
A solution of 4-acetoxybenzoyl chloride (8.37 g) in dry acetonitrile (20 ml) was added to a solution of 2,4,5-trichlorothiophenol (9.00 g) in dry acetonitrile (120 ml) and the mixture stirred at room temperature whilst pyridine (3.41 ml) was added dropwise over 10 minutes. Stirring was continued until the reaction was complete, when ethyl acetate was added and the solution washed with water. Evaporation of the solution, which had been dried over magnesium sulphate, afforded the desired thioester (15.36 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04849419 |
| Source dataset | uspto-grants-1989_07 |
| ORD ID | ord-fd73157b07b94d0194c274f0aa2c0646 |
| Source note | uspto-grants-1989_07 |