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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1607157Generated: October 30, 2026

Ethoxalyl chloride → HCID 44269718, compound

https://huagongshe.com/reaction/1607157

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthoxalyl chlorideHCID 20884—
ReactantHCID 19851977HCID 19851977—
ProductHCID 44269718HCID 44269718—

Reaction Steps

In a manner analogous to that described in Examples 8 and 9, starting from 3-[3-(4-acetyl-3-hydroxy-2-n-propylphenoxy)-propoxy]-2-cyanoaniline, by reaction with chloro-oxalic acid ethyl ester there is obtained N-{3-[3-(4-acetyl-3-hydroxy-2-n-propylphenoxy)-propoxy]-2-cyanophenyl}-oxamic acid ethyl ester having a melting point of 158°-159°, and, by hydrolysis of that compound, N-{3-[3-(4-acetyl-3-hydroxy-2-n-propylphenoxy)-propoxy]-2-cyanophenyl}-oxamic acid is obtained in the form of the triethanolammonium salt having a melting point of 79°-81°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04863942
Source datasetuspto-grants-1989_09
ORD IDord-2837a4c032c942a69da37652bd82256d
Source noteuspto-grants-1989_09