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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 542790Generated: November 1, 2026

Thionyl Chloride → N-(1-methoxy-2,2,2-trichloroethyl)nicotinamide

https://huagongshe.com/reaction/542790

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantN-(2,2,2-trichloro-1-hydroxyethyl)nicotinamideHCID 246390—
ReactantSodium BicarbonateHCID 516892—
ReactantN-(1,2,2,2-tetrachloroethyl)nicotinamideHCID 20207309—
SolventBenzeneHCID 241—
SolventMethanolHCID 887—
SolventTriethylamineHCID 8471—
ProductN-(1-methoxy-2,2,2-trichloroethyl)nicotinamideHCID 13671519—

Reaction Steps

150 ml of benzene was added to 10.0 g of N-(1-hydroxy-2,2,2-trichloroethyl)nicotinamide. 5.3 g of thionyl chloride was added dropwise thereto and the mixture was heated under reflux (60° to 80° C.) for about 5 h under stirring to complete the production of N-(1,2,2,2-tetrachloroethyl)nicotinamide. The reaction liquid was cooled to 30° C. or below. 20 ml of methanol was added to the liquid. 4.0 g of triethylamine was added dropwise to the liquid mixture while it was kept at 5° C. and the obtained mixture was stirred at room temperature for 3 h. Then, the mixture was kept at room temperature overnight. The reaction liquid was poured in an aqueous sodium bicarbonate solution and a benzene layer thus separated was washed with saturated aqueous common salt solution and water and dried over anhydrous sodium sulfate. After concentration, the residue was recrystallized from methanol to obtain 4.8 g of N-(1-methoxy-2,2,2-trichloroethyl)nicotinamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04659722
Source datasetuspto-grants-1987_04
ORD IDord-b386df8ab5ad45a9b76eb7c868224d34
Source noteuspto-grants-1987_04