HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 568623Generated: October 29, 2026
Hydrochloric Acid → HCID 14012556, compound
https://huagongshe.com/reaction/568623
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2,3-Dichloroanisole | HCID 16126 | — |
| Reactant | 2,4-Difluorobenzoyl chloride | HCID 588081 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 14012556 | HCID 14012556 | — |
Reaction Steps
To a solution of 52.23 g of 2,4-difluorobenzoylchloride in 200 ml of 1,2-dichloroethane, 40 g of AlCl3 is added over a 30 minute period. A solution of 48.3 g of 2,3-dichloroanisole in 100 ml 1,2-dichloroethane is added dropwise. There is a slow evolution of gas and the temperature rises to approximately 30° C. The reaction mixture is warmed to 43° C. and the gas continues to evolve for approximately 30 minutes. The mixture is poured over concentrated HCl and ice. The organic layer is separated and the aqueous layer is extracted two times with CHCl3. The combined organic layers are washed with water, dried (Na2SO4) and evaporated to give an oil. Trituration with hexane yields 2,3-dichloro-4-methoxy-2',4'-difluorobenzophenone which is recrystallized from ether, mp 139°-141° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04728662 |
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| Source dataset | uspto-grants-1988_03 |
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| ORD ID | ord-0ee31942d2a543c6b4298e0432fb5505 |
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| Source note | uspto-grants-1988_03 |
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