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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1458878Generated: November 1, 2026

HCID 15083500, compound → HCID 22097678, compound

https://huagongshe.com/reaction/1458878

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 15083500HCID 15083500—
ReactantHCID 22097679HCID 22097679—
SolventO-XyleneHCID 7237—
ProductHCID 22097678HCID 2209767828.5%

Reaction Steps

0.58 g (3.36 mmol) of 4-amino-3-chloro-2-methoxymethylpyridine was added to 0.94 g (3.36 mmol) of 4-(4-chloro-phenoxy)phenylacetyl chloride in 40 ml of xylene, and the mixture was refluxed for 8 hours. After the xylene had been removed in vacuo, the residue was taken up in methylene chloride. The mixture was washed with water and 0.1N aqueous sodium hydroxide solution, the combined aqueous phases were rendered neutral and extracted three times using ethyl acetate, and the ethyl acetate phase was dried over sodium sulfate. After the solvent had been removed in vacuo and the residue purified by column chromatography (silica gel, ethyl acetate:petroleum ether=80:20), 0.40 g of a yellow oil were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05852042
Source datasetuspto-grants-1998_12
ORD IDord-29daa518a14a4e0e943bf81791cf2a76
Source noteuspto-grants-1998_12