HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1850409Generated: October 29, 2026
Water → (2,4,6,7-Tetramethyl-2,3-dihydro-1-benzofuran-2-yl)methanol
https://huagongshe.com/reaction/1850409
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | Phenol, 2,3,5-trimethyl-6-(2-methyl-2-propenyl)- | HCID 10655310 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (2,4,6,7-Tetramethyl-2,3-dihydro-1-benzofuran-2-yl)methanol | HCID 11998626 | 39% |
Reaction Steps
70% m-chloroperbenzoic acid (1.95 g, 7.89 mmol) was added to a solution of toluene (18 mL) containing 2,3,5-trimethyl-6-(2-methylprop-2-en-1-yl)phenol (1.00 g, 5.26 mmol) synthesized in Reference Example 2, and the mixture was stirred at room temperature for 15 hours. The resulting mixture was poured into water, and extraction was performed using ethyl acetate. The extract was washed with 5% sodium sulfite aqueous solution, saturated sodium bicarbonate water and saturated saline, and dried using anhydrous magnesium sulfate. After that, concentration was performed under reduced pressure, and the residue was dissolved in toluene (10 mL). To this solution, trifluoroacetic acid (0.2 mL) was added, and the mixture was stirred at room temperature for 1 hour. After that, the reaction solution was poured into saturated sodium bicarbonate water, and extraction was performed using ethyl acetate. The extract was washed with saturated saline, and dried using anhydrous magnesium sulfate, followed by concentration under reduced pressure. The residue was purified by silica gel chromatography (hexane-ethyl acetate 95:5-85/15) to give 420 mg of the title compound (yield: 39%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08957069B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-081805464a914d6e9ef97ef58fac4390 |
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| Source note | uspto-grants-2015_02 |
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