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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 499876Generated: October 30, 2026

Toluene → 2-(3,5-Diallyloxy-2-ethylphenyl)ethanol

https://huagongshe.com/reaction/499876

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantPotassium sodium tartarateHCID 9855836—
ReactantDiisobutylaluminumhydrideHCID 21225700—
ReactantMethyl 3,5-diallyloxy-2-ethylphenylacetateHCID 23116370—
SolventDichloromethaneHCID 6344—
Product2-(3,5-Diallyloxy-2-ethylphenyl)ethanolHCID 2311648297.3%

Reaction Conditions

Temperature-78 °C

Reaction Steps

Methyl 3,5-diallyloxy-2-ethylphenylacetate (0.84 g, 2.9 mmol) obtained in Example 5, Step 3 was dissolved in dichloromethane (15 mL). After the solution was cooled to −78° C. in an atmosphere of nitrogen, a 1.0 mol/L solution of diisobutylaluminum hydride in toluene (8.4 mL, 8.4 mmol) was added dropwise thereto, followed by stirring at −78° C. for 4 hours. To the reaction mixture was added a saturated aqueous solution of potassium sodium tartrate (50 mL), and the mixture was stirred at room temperature for 3 hours and then extracted with ethyl acetate (0.10 L×2). The organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (ethyl acetate/hexane=1/9-1/1) to obtain 2-(3,5-diallyloxy-2-ethylphenyl)ethanol (0.74 g, 97%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07767693B2
Source datasetuspto-grants-2010_08
ORD IDord-29fef2660c254787850d0c6fabc766af
Source noteuspto-grants-2010_08