HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 605392Generated: October 26, 2026
Methanesulfonic Acid → 4,4,5,7-Tetramethylchroman-2-one
https://huagongshe.com/reaction/605392
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | 3,5-Dimethylphenol | HCID 7948 | — |
| Reactant | Methyl 3-methyl-2-butenoate | HCID 13546 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4,4,5,7-Tetramethylchroman-2-one | HCID 605163 | 92.4% |
Reaction Steps
3,5-Dimethylphenol (5.00 g, 0.0409 mol) and methyl 3,3-dimethylacrylate (5.14 g, 0.045 mol) were added to methanesulfonic acid (5 mL) at room temperature followed by heating at 70° for 17 hours. The reaction was cooled, diluted with water (750 mL), extracted with ethyl acetate (2×200 mL) and the combined organic extracts were washed with saturated aqueous sodium hydrogencarbonate (2×100 mL) and brine (50 mL). The organic phase was dried over magnesium sulfate, filtered, and concentrated by rotary evaporation. Purification by silica gel flash chromatography eluting with methylene chloride afforded the title compound as a beige solid (7.73 g, 0.0378 mol, 92%). 1H NMR (300 MHz, CHLOROFORM-D) δ ppm 1.43 (s, 6 H) 2.27 (s, 3 H) 2.46 (s, 3 H) 2.59 (s, 2 H) 6.74 (s, 2 H). MS (DCI) m/z 205 (M+H)+, 222 (M+NH4)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07910595B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-130812644c67493f977587abbbc20e3f |
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| Source note | uspto-grants-2011_03 |
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