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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1187430Generated: November 2, 2026

Acetic Anhydride → HCID 69184344, compound

https://huagongshe.com/reaction/1187430

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 68536167HCID 68536167—
SolventPyridineHCID 1049—
ProductHCID 69184344HCID 6918434487.1%

Reaction Steps

A mixture of 2-{2-[(3-nitroquinolin4-yl)ammo]ethoxy}ethanol (55.5 g, 0.2 mol), acetic anhydride (37.6 mL, 0.4 mol), and pyridine (250 mL) was heated at reflux for 30 minutes. The solution was allowed to cool to ambient temperature and was concentrated under reduced pressure to remove about 50-75% of the pyridine. The residual solution was poured into water to precipitate the product as an oil which solidified upon stirring. The solid was isolated by filtration, washed with water, and dried. The crude product was recrystallized from 2-propanol (200 mL) to provide 55.6 g of 2-{2-[(3-nitroquinolin-4-yl)amino]ethoxy}ethyl acetate as a bright yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673932B2
Source datasetuspto-grants-2014_03
ORD IDord-aad5b7fc93f8475fa3db3f65e69ad7a8
Source noteuspto-grants-2014_03