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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2248102Generated: October 30, 2026

Acetic Anhydride → HCID 178448614, compound

https://huagongshe.com/reaction/2248102

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 14986963HCID 14986963—
ProductHCID 178448614HCID 178448614—

Reaction Conditions

Temperature20 °C

Reaction Steps

To 50 mL of acetic anhydride was added 11.5 g (0.0477 mole) of 1-(1,1-dimethylethyl)-1H-imidazo-[4,5-c]quinoline-5oxide (produce of Example 25) and the slurry was heated on a steam bath for a few minutes, then allowed to cool to about 20° C. The solid was separated by filtration and washed with an ethanol-hexane mixture. Slurrying with dilute ammonium hydroxide, filtration and washing with water provided solid which has recrystallized from an ethanol-dichloromethane mixture to provide colorless (white) crystals of 1-(1,1-dimethylethyl)-1H-imidazo[4,5-c]quinolin-4-ol, m.p. greater than 300° C. Analysis: Calculated for C14H15N3O: %C, 69.7; %H, 6.3; %N, 17.4; Found: %C, 69.5; %H, 6.3; %N, 17.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05037986
Source datasetuspto-grants-1991_08
ORD IDord-6ea41ea7217343778eb59a612a4489cf
Source noteuspto-grants-1991_08