HuagongsheHuagongshe Chemistry Print Report · For research reference only
P-Chloroacetophenone → HCID 22134085, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | P-Chloroacetophenone | HCID 7467 | — |
| Reactant | Thiophenol | HCID 7969 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22134085 | HCID 22134085 | 81.6% |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
Thiophenol (184 g) was gradually added dropwise to a suspension of 196 g of anhydrous potassium carbonate in 1,000 ml of DMF at room temperature, followed by dropwise addition of 200 g of 4'-chloroacetophenone. The resultant mixture was stirred with heating overnight at 100° C. The reaction mixture was poured into 2,000 ml of ice water and extracted with ethyl acetate. The ethyl acetate layer was washed with water and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. n-Hexane was added to the residue, and the resultant crystals were collected by filtration and washed with n-hexane. Thus was obtained 224 g of 4'-phenylthioacetophenone as crystals (m.p. 48°-50° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05496844 |
| Source dataset | uspto-grants-1996_03 |
| ORD ID | ord-1fc7e5475f574e23afe0939778b6c26d |
| Source note | uspto-grants-1996_03 |