HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1903426Generated: November 2, 2026
3,4,5-Trimethoxytoluene → 6-(11-Acetoxy-1-oxoundecyl)-2,3-dimethoxy-5-methylphenol
https://huagongshe.com/reaction/1903426
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3,4,5-Trimethoxytoluene | HCID 80922 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | 11-Chloro-11-oxoundecyl acetate | HCID 13113786 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | 6-(11-Acetoxy-1-oxoundecyl)-2,3-dimethoxy-5-methylphenol | HCID 20431168 | 79.8% |
Reaction Steps
To a solution (150 ml) of 11-acetoxy-n-undecanoyl chloride (27.6 g) in 1,2-dichloroethane is added aluminum chloride (28 g), and the mixture is stirred at room temperature for 2 hours. The reaction mixture is cooled to 5° C. followed by addition of a solution (50 ml) of 3,4,5-trimethoxytoluene (19.1 g) in 1,2-dichloroethane and the whole mixture is stirred at room temperature for 72 hours. The reaction mixture is then heated to 50°-60° C. and stirred for 30 minutes. After cooling, 300 ml of ice water is added to the reaction mixture and the product is extracted with dichloromethane. The dichloromethane layer is washed with water and dried over anhydrous magnesium sulfate, and the solvent is distilled off to give a light-yellow oil of 6-(11-acetoxy-1-oxoundecyl)-2,3-dimethoxy-5-methylphenol (33 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04436753 |
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| Source dataset | uspto-grants-1984_03 |
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| ORD ID | ord-8ef1e1c66ddf456eb36f569ded189789 |
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| Source note | uspto-grants-1984_03 |
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