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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1863097Generated: October 30, 2026

Sodium Iodide → HCID 86736121, compound

https://huagongshe.com/reaction/1863097

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantMorpholineHCID 8083—
ReactantHCID 54028532HCID 54028532—
ReactantHCID 86736122HCID 86736122—
SolventMethyl Ethyl KetoneHCID 6569—
ProductHCID 86736121HCID 86736121—

Reaction Steps

A solution of 7.6 g. of o-benzyl-p-chlorophenylglyoxylic acid (3-chloropropyl)methylamide in 40 ml. of ethyl methyl ketone is treated with 3.0 g. of sodium iodide and 3.5 g. of morpholine and the mixture is boiled at reflux for 30 hours. After concentration under reduced pressure, the residue is partitioned between water and methylene chloride, the organic phase washed with water, dried over sodium sulfate and concentrated to dryness. The residual oily base is purified on 500 g. of aluminum oxide using methylene chloride/ethyl acetate (4:1) for the elution, dissolved in diethyl ether and treated with excess ethereal hydrochloric acid. The hydrochloride which crystallizes out is recrystallized from isopropanol/diethyl ether, and there is obtained 4.9 g. of o-benzoyl-p-chlorophenylglyoxylic acid [3-(morpholino)propyl]methylamide hydrochloride in the form of light yellow crystals having a melting point of 169°-172° C. (decomposition).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04167632
Source datasetuspto-grants-1979_09
ORD IDord-08b91221002c476fbeb0873f12375c78
Source noteuspto-grants-1979_09