HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1047195Generated: November 2, 2026
2-Methylacetophenone → 2-(2-Methylphenyl)propan-2-ol
https://huagongshe.com/reaction/1047195
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Methylacetophenone | HCID 11340 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(2-Methylphenyl)propan-2-ol | HCID 244005 | 88% |
Reaction Steps
Under the protection by nitrogen, ortho-methylphenylethanone (134 g, 1.0 mol) is dissolved in 1000 ml of tetrahydrofuran and then cooled to −5° C., into which 2 M methylmagnesium bromide in tetrahydrofuran (550 ml) is slowly added dropwise at below 0° C. After the addition, the reactant solution is stirred at room temperature for 3 hours under the detection of TLC. When the reaction is complete, 200 ml of saturated NH4Cl solution is slowly added dropwise into the reactant solution and stirred until no bubbling from the solution. The resulted solution is then extracted by dichloromethane (500 ml×3), the extracts are combined, dried by anhydrous sodium sulfate, absorbed by activated carbon, filtered, and then the solvent is distilled out using rotary evaporator to obtain 132 g of 2-ortho-methylphenyl-2-propanol as a light yellow sticky liquid, with a yield of 88%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08569508B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-db14f30b0fdd40579c84c3f9bbc33686 |
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| Source note | uspto-grants-2013_10 |
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