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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 903856Generated: October 31, 2026

1-Bromo-3-chlorobenzene → HCID 23335278, compound

https://huagongshe.com/reaction/903856

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-3-chlorobenzeneHCID 7928—
Reactant2-Methyl-5-hydroxypyridineHCID 14275—
ReactantPotassiumHCID 5462222—
CatalystCopperHCID 23978—
SolventEthanolHCID 702—
SolventDimethylformamideHCID 6228—
ProductHCID 23335278HCID 23335278—

Reaction Steps

3 g of a potassium salt of 5-hydroxy-2-methylpyridine, 3.83 g of m-bromochlorobenzene and 200 mg of a copper powder were suspended in 8 ml of dimethylformamide, followed by allowing the mixture to react in a nitrogen gas stream at 130° C. for 13 hours while stirring. The reaction mixture was diluted with 40 ml of ethanol and filtered. The filtrate was immediately concentrated, and 80 ml of chloroform was added to the residue. The mixture was washed with a 0.01 N aqueous sodium hydroxide solution. The chloroform layer was washed with water, dried with anhydrous sodium sulfate and dried to solidify to obtain 2.96 g of oily 5-(m-chlorophenoxy)-2-methylpyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04229448
Source datasetuspto-grants-1980_10
ORD IDord-a716f55957bf49fb8df6084c78376103
Source noteuspto-grants-1980_10