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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1871867Generated: November 2, 2026

2,3,6-Trichloro-5-(trifluoromethyl)pyridine → 2,5-Dichloro-6-methoxy-3-trifluoromethylpyridine

https://huagongshe.com/reaction/1871867

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3,6-Trichloro-5-(trifluoromethyl)pyridineHCID 2760690—
ReactantSodium MethoxideHCID 10942334—
Solventtert-Butyl methyl etherHCID 15413—
Product2,5-Dichloro-6-methoxy-3-trifluoromethylpyridineHCID 18689510—

Reaction Conditions

Temperature20 °C

Reaction Steps

10.8 g (0.06 mol) of 30% strength sodium methoxide solution were added to 15 g (0.06 mol) of 2,3,6-trichloro-5-trifluoromethylpyridine in 200 ml of methyl tert-butyl ether at 0-5° C. with stirring in the course of 20 minutes and the mixture was subsequently stirred at the same temperature for 30 minutes. After warming to 20° C., the resulting fine precipitate was filtered off with suction and washed with methyl tert-butyl ether. The organic filtrate was washed with water, dried and concentrated, 14.3 g (97% of theory) of the title compound of n25D =1.4890 being obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06107253
Source datasetuspto-grants-2000_08
ORD IDord-073c19489dc54292b2d1dc8b874290c5
Source noteuspto-grants-2000_08