HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methylbenzaldehyde → Benzal chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methylbenzaldehyde | HCID 7725 | — |
| Reactant | Phosphorus pentachloride | HCID 24819 | — |
| Reactant | 1,4-Bis(dichloromethyl)benzene | HCID 81884 | — |
| Product | Benzal chloride | HCID 7411 | 96.5% |
Reaction Steps
JP79125629 (1979) discloses a method for preparing α,α,α′,α′-tetrachloro-p-xylene by reacting 4-methyl benzaldehyde with PCl5, forming an intermediate product 4-methyl, 1-(dichloromethyl)benzene, and conducting a photochlorination reaction. This prior art method has the following reaction formula: The abovementioned reaction is a two-step reaction. Even though the first step reaction has a yield of 96.5%, the second step reaction has a very low yield. The product mixture is very difficult to be purified.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06992231B2 |
| Source dataset | uspto-grants-2006_01 |
| ORD ID | ord-13c635c5862a412cac2813753893a5cc |
| Source note | uspto-grants-2006_01 |