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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2412841Generated: November 1, 2026

3,4,5-Trimethoxytoluene → HCID 12832659, compound

https://huagongshe.com/reaction/2412841

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4,5-TrimethoxytolueneHCID 80922—
ReactantAluminum(III) ChlorideHCID 6451240—
ReactantHCID 20254621HCID 20254621—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 12832659HCID 1283265946.6%

Reaction Steps

To a solution of 18-acetoxy-n-octadecanoyl chloride (11 g) in 1,2-dichloroethane (50 ml) is added aluminum chloride (7 g) and the mixture is stirred at room temperature for 2 hours. This reaction mixture is cooled to 5° C. and a solution of 3,4,5-trimethoxytoluene (6.2 g) in 1,2-dichloroethane (20 ml) is added. The mixture is stirred at room temperature for 72 hours. Then, this reaction mixture is heated to 50° C.-60° C. and stirred for 30 minutes. After cooling, ice-water is added to the reaction mixture and the product is extracted with dichloromethane. The dichloromethane layer is washed with water and the solvent is distilled off to recover an oil (12.1 g). This oil is dissolved in methanol (150 ml) followed by addition of sodium hydroxide (5.2 g). The mixture is stirred at room temperature for 2 hours, at the end of which time it is neutralized with 5N--HCl and the solvent is distilled off. The resultant crude crystals are rinsed with water and recrystallized from dichloromethane-ether (1:1). The above procedure yields 6-(18-hydroxy-1-oxooctadecyl)-2,3-dimethoxy-5-methylphenol (6.4 g) as colorless needles, m.p. 101° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04495104
Source datasetuspto-grants-1985_01
ORD IDord-d0b247b080574b7692a210a49b241cb1
Source noteuspto-grants-1985_01