HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 263924Generated: October 25, 2026
Sulfuric Acid → 2H-1-Benzopyran-6-ol, 3,4-dihydro-2-methoxy-2,5,7,8-tetramethyl-
https://huagongshe.com/reaction/263924
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Methyl vinyl ketone | HCID 6570 | — |
| Reactant | Trimethyl orthoformate | HCID 9005 | — |
| Reactant | Trimethylhydroquinone | HCID 12785 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2H-1-Benzopyran-6-ol, 3,4-dihydro-2-methoxy-2,5,7,8-tetramethyl- | HCID 103763 | 92.6% |
Reaction Steps
Concentrated sulfuric acid (0.8 mL) was added dropwise to a solution of trimethyl orthoformate (Aldrich, 48.5 g, 457.0 mmol) and trimethyl hydroquinone (Aldrich, 50.0 g, 328.5 mol) in methanol (200 mL), cooled by a water/ice bath. Methyl vinyl ketone (Aldrich, 46.05 g, 657.0 mmol) was added slowly (1.5 h) to the reaction mixture while the reaction mixture was cooled by an ice/water bath. A pasty slurry formed. The reaction mixture was allowed to come to ambient temperature and was stirred at ambient temperature for 48 h. The reaction mixture was diluted with diethyl ether (600 mL) and the resulting solution was extracted with water (2×200 mL) and saturated aqueous sodium bicarbonate (2×100 mL). The organic solution was dried (sodium sulfate) and concentrated in vacuo to give a tan solid. The solid was recrystallized from methanol to give 71.8 g (92.6%) of the desired product as a tan solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05646149 |
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| Source dataset | uspto-grants-1997_07 |
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| ORD ID | ord-e869cbf248364ce393243da6e7bfa8b3 |
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| Source note | uspto-grants-1997_07 |
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