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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTolueneHCID 1140—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantPhenol, 2,3,5-trimethyl-6-(2-methyl-2-propenyl)-HCID 10655310—
SolventEthyl AcetateHCID 8857—
Product(2,4,6,7-Tetramethyl-2,3-dihydro-1-benzofuran-2-yl)methanolHCID 1199862639%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957069B2
Source datasetuspto-grants-2015_02
ORD IDord-081805464a914d6e9ef97ef58fac4390
Source noteuspto-grants-2015_02