HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 920527Generated: October 31, 2026
Acetyl chloride → 2'-CHLORO-4'-HYDROXYACETOPHENONE
https://huagongshe.com/reaction/920527
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | 3-Chloroanisole | HCID 17833 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2'-CHLORO-4'-HYDROXYACETOPHENONE | HCID 11252402 | 64.9% |
Reaction Steps
To a mixture of AlCl3 (42.08 g; 315.60 mmol) in CH2Cl2 (300 mL) was added dropwise 3-chloroanisole (22.50 g; 157.80 mmol), at −30° C. To the resulting mixture was added dropwise a solution of AcCl (10.50 mL; 147.63 mmol) in CH2Cl2 (100 mL) at such a rate to keep the temperature below −15° C. The resulting mixture was stirred for 4 hours at −10° C. Subsequently, the mixture was poured onto ice and extracted with CH2Cl2. The combined organic layers, were dried (MgSO4), filtered, and concentrated in vacuo. The residue was purified by column chromatography (SiO2, Et2O/hexanes 1:9) to afford 1-(2-chloro-4-methoxy-phenyl)-ethanone (17.68 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09273017B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-1a6140baa4f54a6897e1989be57b34fe |
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| Source note | uspto-grants-2016_03 |
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