HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 652914Generated: October 27, 2026
Hydrochloric Acid → 2,3-Dichloro-2',4-dimethoxybenzophenone
https://huagongshe.com/reaction/652914
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2,3-Dichloroanisole | HCID 16126 | — |
| Reactant | 2-Methoxybenzoyl chloride | HCID 88969 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 2,3-Dichloro-2',4-dimethoxybenzophenone | HCID 14012570 | — |
Reaction Steps
To a mixture of 3.9 g of AlCl3 and 4.67 g of 2,3-dichloroanisole in 70 ml of 1,2-dichloroethane at -10° C., 5 g of o-methoxybenzoyl chloride is added dropwise. The mixture is stirred for 2.5 hours and is gradually warmed to 5° C. The reaction mixture is poured into concentrated HCl and ice. The mixture is stirred one half hour to decompose the complex. The aqueous layer is extracted with additional organic solvent. The combined organic layers are washed until neutral, dried over Na2SO4 and evaporated to give an oil which solidifies on trituration with hexane. The crude product is recrystallized from 95% ethanol giving 2,3-dichloro-2',4-dimethoxybenzophenone, mp 94°-96° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04673746 |
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| Source dataset | uspto-grants-1987_06 |
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| ORD ID | ord-618890a8d0ac4423a47d5ad2083e6379 |
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| Source note | uspto-grants-1987_06 |
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