HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2190464Generated: October 30, 2026
Methyl iodide → Methyl 3-(2-methyl-1-oxopropan-2-yl)benzoate
https://huagongshe.com/reaction/2190464
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-(1,1-Dimethyl-2-oxoethyl)benzoic acid | HCID 86646028 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Methyl 3-(2-methyl-1-oxopropan-2-yl)benzoate | HCID 86646029 | — |
Reaction Steps
To a solution of 3-(1,1-dimethyl-2-oxoethyl)benzoic acid in acetone (60 mL) were added potassium carbonate (3.78 g, 27.3 mmol) and methyl iodide (3.40 mL, 54.6 mmol), and the mixture was stirred at 60° C. for 5 hr. The insoluble material was filtered off, and the filtrate was concentrated under reduced pressure. To the obtained residue was added saturated aqueous sodium hydrogencarbonate solution (50 mL), and the mixture was extracted with ethyl acetate (100 mL, 30 mL). The combined organic layer was washed with saturated brine (20 mL), and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the filtrate was concentrated under reduced pressure to give methyl 3-(1,1-dimethyl-2-oxoethyl)benzoate as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08324395B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-f95fdac6cfc74cd7a4ac0b1e16d118e5 |
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| Source note | uspto-grants-2012_12 |
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