HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,4-Dichlorobenzene → 2,5-Dichlorobenzophenone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,4-Dichlorobenzene | HCID 4685 | — |
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Product | 2,5-Dichlorobenzophenone | HCID 458188 | 50% |
Reaction Steps
Starting material ratios as low as 1.1/1.3/1 (moles of AlCl3 :1,4-dichlorobenzene:benzoyl chloride) have been found sufficient to produce 2,5-dichlorobenzophenone in about 50% yield under the conditions provided by the present invention; the same ratio of starting materials has been found to give a 64% yield of 2,5-dichlorobenzophenone if the benzoyl chloride is added slowly to a mixture of AlCl3, 1,4-dichlorobenzene and a small amount of benzoyl chloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05210313 |
| Source dataset | uspto-grants-1993_05 |
| ORD ID | ord-a0a6697ef4f34384bc2fb4b978b451d0 |
| Source note | uspto-grants-1993_05 |