HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1653615Generated: November 2, 2026
Hydrochloric Acid → 2,5-Dichloro-4'-phenoxybenzophenone
https://huagongshe.com/reaction/1653615
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diphenyl Ether | HCID 7583 | — |
| Reactant | 2,5-Dichlorobenzoyl chloride | HCID 17945 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2,5-Dichloro-4'-phenoxybenzophenone | HCID 12081059 | 73% |
Reaction Steps
To a 22 L open-mouth round bottom flask fitted with a three-necked flange head, a mechanical stirrer, a nitrogen inlet and an outlet connected to a HCl scrubbing tower, is added 2,5-dichlorobenzoic chloride (4500 g, 21.5 mol) and phenyl ether (5489 g, 32.3 mol). The solution is cooled in ice to 5° C. under stirring, and aluminum chloride (3700 g, 27.8 mol) is added slowly, over a period of about 10 minutes. The temperature of the reaction mixture is about 35° C. after the addition. The mixture is then stirred for about 30 minutes and poured into about 20 gallons of ice water. The large reddish mass is dissolved by adding about 12 L of methylene chloride and stirring. The organic layer is separated and the aqueous layer is extracted with some methylene chloride. After methylene chloride is removed from the combined organic layer by distillation, the residue is recrystallized twice from cyclohexane (2×10 L), washed with cooled hexane, air dried, and then vacuum dried, to afford 5387 g monomer (73%). The mother liquor is kept for later recovery of remaining product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05403675 |
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| Source dataset | uspto-grants-1995_04 |
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| ORD ID | ord-3ddf9063c201453fac84204e221a006a |
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| Source note | uspto-grants-1995_04 |
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