HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1359460Generated: November 1, 2026
Methyl iodide → 4-(4-Methoxyphenyl)cyclohexanone
https://huagongshe.com/reaction/1359460
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-(4'-Hydroxyphenyl)cyclohexanone | HCID 4598916 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 4-(4-Methoxyphenyl)cyclohexanone | HCID 10976581 | 100% |
Reaction Steps
A solution of 4-(4-hydroxyphenyl)cyclohexanone (5.0 g, 26.3 mmol) in acetone (100 mL) was treated with K2CO3 (14.5 g, 105 mmol, 4 equiv) and iodomethane (4.9 mL, 11.2 g, 78.6 mmol, 3 equiv.). The reaction was heated at 65° C. overnight. After the solvent was removed, the residue was treated with H2O and extracted with EtOAc. The organic extracts were combined and washed with brine, dried over Na2SO4 and concentrated in vacuum to give the spectroscopically pure 4-(4-methoxyphenyl)cyclohexanone (5.34 g, 100%). 1H NMR(CDCl3) 7.16 (dt, 2H), 6.87 (dt, 2H), 3.78 (s, 3H), 2.99 (tt, 1H), 2.47-2.53 (m, 4H), 2.20 (m, 2H) and 1.83-1.98 (m, 2H); MS (electrospray) m/e, 205 (M+1)+, Calcd for C13H16O2, 204.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06600015B2 |
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| Source dataset | uspto-grants-2003_07 |
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| ORD ID | ord-0b914538b1ac4ac880ad1922f32f6734 |
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| Source note | uspto-grants-2003_07 |
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