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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Potassium sodium tartarate | HCID 9855836 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Reactant | Methyl 3,5-diallyloxy-2-ethylphenylacetate | HCID 23116370 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(3,5-Diallyloxy-2-ethylphenyl)ethanol | HCID 23116482 | 97.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07767693B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-29fef2660c254787850d0c6fabc766af |
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| Source note | uspto-grants-2010_08 |
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