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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1703345Generated: October 30, 2026

4-Methoxyphenol → HCID 12833251, compound

https://huagongshe.com/reaction/1703345

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethoxyphenolHCID 9015—
ReactantPotassium HydroxideHCID 14797—
Reactant2-Chloro-6(dichloromethyl)pyridineHCID 174111—
ReactantHCID 178418361HCID 178418361—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
ProductHCID 12833251HCID 12833251—

Reaction Conditions

Temperature25 °C

Reaction Steps

A mixture of 15.04 grams (g) (0.076 mole (m)) of 2-dichloromethyl-6-chloropyridine, 39.50 g (0.32 m) of p-methoxyphenol and 18.14 g (0.32 m) of potassium hydroxide in 100 milliliters (ml) of dimethylsulfoxide was heated, with stirring, for 72 hours. The resulting mixture was cooled to 25° C., diluted with water and extracted with 1,1,1-trichloroethane. The extract was washed with water, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The concentrate was subjected to Kugelrohr distillation removing as impurities any material boiling up to 200° C. at 0.05-1 millimeter of mercury (mm). The 2-[bis-(4-methoxyphenoxy)methyl]-6-(4-methoxyphenoxy)pyridine product was removed as the residue of the distillation and was a brown thick oil. The product was obtained in a yield of 25.3 g and upon analysis, was found to have carbon, hydrogen and nitrogen contents of 70.80, 5.37 and 3.09 percent, respectively, as compared with the theoretical contents of 70.59, 5.45 and 3.05 percent, respectively, as calculated for the above named compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04351943
Source datasetuspto-grants-1982_09
ORD IDord-071fde58b3f94bc8b756f892b54af42e
Source noteuspto-grants-1982_09