HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2257125Generated: November 3, 2026
Hydrochloric Acid → 1-(5-Chloro-2-methoxy-4-methylphenyl)-ethanone
https://huagongshe.com/reaction/2257125
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | 1-Chloro-4-methoxy-2-methylbenzene | HCID 458156 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 1-(5-Chloro-2-methoxy-4-methylphenyl)-ethanone | HCID 2757638 | 21.5% |
Reaction Steps
A suspension of 2.12 g of AlCl3 in 20 ml of CCl4 is cooled to 0° C. under a nitrogen atmosphere, and a solution of 1.25 g of acetyl chloride in 10 ml of CCl4 is added dropwise. A solution of 2.5 g of 2-chloro-5-methoxytoluene in 10 ml of CCl4 is then added dropwise, and the mixture is left stirring for 2 hours while the temperature is allowed to rise to r.t. The mixture is poured into a mixture of concentrated HCl and ice, the resulting mixture is extracted with DCM, the organic phase is dried over magnesium sulphate and the solvent is evaporated off under vacuum. The residue is chromatographed on silica H, eluting with a DCM/heptane (70:30; v/v) mixture. 0.68 g of the expected product, m.p.=83° C., is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05656648 |
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| Source dataset | uspto-grants-1997_08 |
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| ORD ID | ord-6681a9d41f1547578f55d5fbb8ba77ce |
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| Source note | uspto-grants-1997_08 |
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