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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1957249Generated: October 31, 2026

Ethanol → 3-Chloro-2-(4-chloro-3-methoxyphenyl)-6-ethoxy-5-trifluoromethylpyridine

https://huagongshe.com/reaction/1957249

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantPotassium HydroxideHCID 14797—
Reactant3,6-Dichloro-2-(4-chloro-3-methoxyphenyl)-5-trifluoromethylpyridineHCID 19068780—
Product3-Chloro-2-(4-chloro-3-methoxyphenyl)-6-ethoxy-5-trifluoromethylpyridineHCID 19068743—

Reaction Steps

6.5 g (18 mmol) of 3,6-dichloro-2-(4-chloro-3-methoxyphenyl)-5-trifluoromethylpyridine and 6.1 g (109 mmol) of potassium hydroxide in 100 ml of ethanol were stirred at 23° C. for 41 h. The solvent was then removed by distillation and the residue was taken up in 100 ml of dilute hydrochloric acid. Extraction was carried out three times with 100 ml of methylene chloride each time. The combined extracts were dried over sodium sulfate and then concentrated. Yield: 6.3 g (85%) of a colorless oil (purity about 90%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05783522
Source datasetuspto-grants-1998_07
ORD IDord-5a5a1f6c5f4d44659b8173e289716c4c
Source noteuspto-grants-1998_07