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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1494308Generated: November 2, 2026

Ammonia → 2-(6-Chloro-pyridin-2-yl)-morpholin-5-one

https://huagongshe.com/reaction/1494308

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantHydrochloric AcidHCID 313—
ReactantEthyl chloroacetateHCID 7751—
ReactantSodium hydrideHCID 24758—
Reactant2-Amino-1-(6-chloropyridin-2-yl)ethan-1-olHCID 14578852—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product2-(6-Chloro-pyridin-2-yl)-morpholin-5-oneHCID 14578853—

Reaction Steps

6 g (0.0347 mol) of 2-hydroxy-2-(2-chloro-pyridin-6-yl)-ethanamine are dissolved in 160 ml of absolute toluene and mixed with 2.2 g (0.047 mol) of 50% sodium hydride in oil and stirred for 40 minutes at ambient temperature. Then 4.16 g (0.034 mol) of ethyl chloroacetate are added dropwise. The reaction mixture is stirred for 18 hours at ambient temperature and then carefully mixed with 10 ml of ethanol and 30 ml of water and subsequently acidified with dilute hydrochloric acid. The reaction solution is made alkaline with ammonia and extracted with methylene chloride. The organic phase is dried over sodium sulphate, concentrated by evaporation and the residue is purified over a silica gel column using ethyl acetate as eluant.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05026702
Source datasetuspto-grants-1991_06
ORD IDord-d06624a87e1849a28fb38a7422dc2ee7
Source noteuspto-grants-1991_06