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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 542792Generated: October 31, 2026

2-Methoxyethylamine → N-(2-methoxyethylamino-2,2,2-trichloroethyl)nicotinamide

https://huagongshe.com/reaction/542792

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethoxyethylamineHCID 8018—
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—
SolventTriethylamineHCID 8471—
ProductN-(2-methoxyethylamino-2,2,2-trichloroethyl)nicotinamideHCID 1375290341.3%

Reaction Steps

150 ml of benzene was added to 5.0 g of N-(1-hydroxy-2,2,2-trichloroethyl)nicotinamide. 2.6 g of thionyl chloride was added dropwise to the mixture under stirring and the obtained mixture was heated under stirring at 60° to 80° C. for about 5 h to complete the production of N-(1,2,2,2-tetrachloroethyl)nicotinamide. The reaction solution was cooled to a temperature of 30° C. or below. 1.4 g of 2-methoxyethylamine was added thereto and then 3.7 g of triethylamine was added dropwise to the liquid mixture kept at 5° C. After stirring at room temperature for 3 h, the mixture was left to stand at room temperature overnight. The reaction solution was poured in an aqueous sodium bicarbonate solution. A benzene layer thus separated was washed with a saturated aqueous common salt solution and water and dried over anhydrous sodium sulfate. After concentration, the residue was recrystallized from a solvent mixture of n-hexane and ethyl acetate to obtain 2.5 g of N-(2-methoxyethylamino-2,2,2-trichloroethyl)nicotinamide. m.p. 75° to 77° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04659722
Source datasetuspto-grants-1987_04
ORD IDord-228489d045564f03a1dc20bb211301a1
Source noteuspto-grants-1987_04