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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 903857Generated: October 31, 2026

4-Bromoanisole → HCID 23335283, compound

https://huagongshe.com/reaction/903857

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromoanisoleHCID 7730—
Reactant2-Methyl-5-hydroxypyridineHCID 14275—
ReactantPotassiumHCID 5462222—
CatalystCopperHCID 23978—
SolventMethanolHCID 887—
SolventDimethylacetamideHCID 31374—
ProductHCID 23335283HCID 23335283—

Reaction Steps

4 g of a potassium salt of 5-hydroxy-2-methylpyridine was suspended in 10 ml of dimethylacetamide, and 5.1 g of p-methoxybromobenzene and 450 mg of a copper powder were added to the suspension, followed by allowing the mixture to react in a nitrogen stream at 140° C. for 14 hours. The reaction mixture was diluted with 50 ml of methanol and filtered, and the filtrate was immediately dried to a solid. 100 ml of ethyl acetate was added to the residue, and the mixture was washed with 50 ml of an aqueous sodium hydroxide solution at pH 9. The ethyl acetate layer was washed with water, dried with anhydrous sodium sulfate and immediately dried to obtain 3.9 g of oily 5-(p-methoxyphenoxy)-2-methylpyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04229448
Source datasetuspto-grants-1980_10
ORD IDord-44b688a30279464a8bd6638c4bbf2c6b
Source noteuspto-grants-1980_10