HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → 4-(2-Phenylethenyl)benzoyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 5162089 | HCID 5162089 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(2-Phenylethenyl)benzoyl chloride | HCID 53817288 | 84% |
Reaction Steps
15.1 g (67.4 mmols) of stilbene-4-carboxylic acid, 10.0 g (84.25 mmols) of thionyl chloride, 150 ml of toluene and 0.18 ml of N,N-dimethylformamide are stirred at 70° C. for 3 hours. The reaction mixture is then evaporated and the crude product is recrystallised from n-hexane/cyclohexane. 13.7 g (84% of theory) of stilbene-4-carboxylic acid chloride are obtained in the form of white crystals; melting point 131.2° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04918215 |
| Source dataset | uspto-grants-1990_04 |
| ORD ID | ord-304ea038ff9645ef97ab479614790942 |
| Source note | uspto-grants-1990_04 |