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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1733292Generated: November 2, 2026

Sodium hydride → N-(4-methyl-2-thiazolyl)-N-(2-dimethylaminoethyl)acetamide

https://huagongshe.com/reaction/1733292

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant2-Acetamido-4-methylthiazoleHCID 280907—
ReactantN,N-Dimethylaminoethyl chloride hydrochlorideHCID 11636816—
SolventDimethylformamideHCID 6228—
ProductN-(4-methyl-2-thiazolyl)-N-(2-dimethylaminoethyl)acetamideHCID 12791196—

Reaction Steps

The reaction is run under a nitrogen atmosphere. To a stirred solution of 31.2 g. (0.20 mole) of 2-acetamido-4-methylthiazole in 300 ml. of DMF is added 9.6 g. (0.20 mole) of a 50% suspension of sodium hydride in mineral oil. The reaction is stirred for 1/2 hour as the temperature spontaneously rises to 50° C. The reaction is cooled to 35° to 40° C. and a further 12.0 g. (0.25 mole) of sodium hydride suspension added followed by 36.0 g. (0.25 mole) of 2-dimethylaminoethyl chloride HCl, added portionwise for 10 to 15 minutes. The mixture is stirred at room temperature for about 1 hour and then at steam bath temperature for 20 hours. The tan mixture is cooled to ambient temperature and filtered to remove salts. The filtrate is concentrated under reduced pressure at steam bath temperature. This gives 46.4 g. of crude product as a brown oil (containing mineral oil (10.8 g.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04241072
Source datasetuspto-grants-1980_12
ORD IDord-79cad6fa78b048ad966418036c55b961
Source noteuspto-grants-1980_12