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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1769642Generated: October 31, 2026

Acetic Anhydride → HCID 15044008, compound

https://huagongshe.com/reaction/1769642

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 178507165HCID 178507165—
ProductHCID 15044008HCID 1504400852%

Reaction Steps

A solution of 9-amino-3,4-dihydroacridin-1(2H)-one N-oxide (5.4 g) and acetic anhydride (60 ml) was heated to reflux and then concentrated. The residue was stirred in saturated sodium bicarbonate solution for one hr. The mixture was filtered and the filter cake was washed with water and dried under vacuum at 40° C. for three hrs to yield 1.93 g of product, mp 208° C. (dec). An additional 1.38 g, mp 208° C. (dec), of product was obtained by extraction of the tiltrate with ethyl acetate, evaporation of ethyl acetate extract, and trituration of the residue with diethyl ether; total 52% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05382594
Source datasetuspto-grants-1995_01
ORD IDord-3e17ab538baa4ea69a93a016a295dfb3
Source noteuspto-grants-1995_01