HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1957489Generated: October 27, 2026
Hydrochloric Acid → 2,4,5-Trimethoxyacetophenone
https://huagongshe.com/reaction/1957489
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | 1,2,4-Trimethoxybenzene | HCID 67284 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2,4,5-Trimethoxyacetophenone | HCID 74560 | 50% |
Reaction Steps
To methylene chloride, 47.5 g of aluminum chloride were added, followed by the addition of 30 g of 2,4,5-trimethoxybenzene and then 13 ml of acetyl chloride under ice cooling. The resulting mixture was stirred at room temperature for 6 hours. After the completion of the reaction, 1N hydrochloric acid was added to the reaction mixture under ice cooling. The resulting mixture was then extracted with methylene chloride. The extract so obtained was washed successively with 1N hydrochloric acid, a 1N aqueous solution of sodium hydrochloride and saturated saline and then dried over anhydrous magnesium sulfate. The organic layer was concentrated under reduced pressure. The crude product so obtained was washed with ethanol, whereby 18.6 g of 2',4',5'-trimethoxyacetophenone were obtained (yield: 50%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05786355 |
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| Source dataset | uspto-grants-1998_07 |
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| ORD ID | ord-9f16f478769448b1975ecd0b89166eed |
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| Source note | uspto-grants-1998_07 |
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