HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1252797Generated: November 2, 2026
Methyl iodide → 2-(2-Fluoro-4-methoxyphenyl)-2-propanol
https://huagongshe.com/reaction/1252797
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 2'-Fluoro-4'-methoxyacetophenone | HCID 592821 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-(2-Fluoro-4-methoxyphenyl)-2-propanol | HCID 13493844 | 80.9% |
Reaction Steps
17.75 g (0.125 mole) methyliodide are dissolved in diethylether and the resulting solution is added dropwise with stirring to 3.04 g magnesium chips in 15 ml anhydrous ether. The mixture is then heated under reflux for 30 minutes, followed by the dropwise addition with stirring of a solution of 16.82 g (0.1 mole) 2-fluoro-4-methoxy-acetophenone in diethylether. After heating under reflux for 2 hours, the reaction mixture is cooled, poured onto ice and the corresponding deposit dissolved by addition of aqueous NH4Cl solution. The ether phase is separated off, the aqueous phase is extracted with ether, the combined ether phases are washed with aqueous solutions of NaHSO3, NaHCO3 and then with pure water, dried over Na2SO4 and the ether removed. Distillation of the residual oil in a high vacuum gives 14.9 g 2-(2-fluoro-4-methoxyphenyl)-2-propanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04745233 |
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| Source dataset | uspto-grants-1988_05 |
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| ORD ID | ord-5b92d93daf3f4b858717dc80c624a6c3 |
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| Source note | uspto-grants-1988_05 |
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