HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → 4-Formylbenzoyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | 4-Formylbenzoic acid | HCID 12088 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 4-Formylbenzoyl chloride | HCID 12424620 | — |
Reaction Steps
The title substance was synthesized as follows: 300 ml of thionyl chloride was dropped into a mixture of 358 g of commercially available terephthalaldehydic acid with 700 ml of toluene and 2 g of pyridine, and the solution was heated under reflux slowly until a homogeneous reaction solution was obtained. After the solution was cooled to room temperature, unreacted thionyl chloride and toluene as a solvent were distilled off in vacuum. Terephthalaldehydic acid chloride (b.p. 133°-135° C./15 Torr) was obtained by the vacuum distillation of the remaining reaction product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04576732 |
| Source dataset | uspto-grants-1986_03 |
| ORD ID | ord-5a064abc5ffa42899e5dd959a8912764 |
| Source note | uspto-grants-1986_03 |