HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1067113Generated: October 30, 2026
Hydrochloric Acid → 2-(3-Methoxy-2-methylbenzyl)cyclohexanone
https://huagongshe.com/reaction/1067113
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 21196457 | HCID 21196457 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-(3-Methoxy-2-methylbenzyl)cyclohexanone | HCID 18367419 | 56.7% |
Reaction Steps
To a solution of 2-[hydroxy-(3-methoxy-2-methylphenyl)-methyl]cyclohexanone (1.85 g) in THF (20 ml) was added conc. HCl (0.5 ml) at 5° C. and the mixture was stirred at room temperature for 1 hour. The reaction mixture was diluted with EtOAc, washed with saturated sodium hydrogen carbonate, water, and brine, dried over magnesium sulfate, evaporated in vacuo. The residue was dissolved in MeOH (30 ml) and 10% Pd/C (wet) (400 mg) was added. The mixture was stirred under hydrogen atmosphere at room temperature for 2 hours. The catalyst was removed by filtration and the filtrate was evaporated. The residue was pufified by silica gel column chromatography (hexane-EtOAc 12:1 to 8:1) to give 2-(3-methoxy-2-methylbenzyl)cyclohexanone (980.6 mg) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06245790B1 |
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| Source dataset | uspto-grants-2001_06 |
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| ORD ID | ord-b03804560209470a91d2a6b85f3f9864 |
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| Source note | uspto-grants-2001_06 |
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