Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 464824Generated: October 30, 2026

Water → HCID 70453742, compound

https://huagongshe.com/reaction/464824

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPyridineHCID 1049—
ReactantTolueneHCID 1140—
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 178463792HCID 178463792—
CatalystZincHCID 23994—
ProductHCID 70453742HCID 70453742—

Reaction Steps

A mixture of 10.0 g of 1,3-diamino-7-diethylamino-8-methylphenoxazin-5-ium chloride (Brilliant Cresyl Blue, Eastman Kodak), 50.0 ml of acetic anhydride, 10.0 g of zinc dust and 10.0 ml of pyridine was maintained at 85° to 90° C. for approximately one hour. After cooling to room temperature, the reaction mixture was poured into a mixture of water and toluene and the resulting water layer was separated and discarded. The toluene solution was washed twice, first with water and then with saturated sodium chloride solution. The toluene was removed by evaporation at reduced pressure. The resulting residue was recrystallized from isopropanol and the solid obtained was recrystallized from ethanol to obtain 0.2 g of 1,9-dimethyl-4-acetamido-8-diethylaminoimidazophenoxazine (Formula I: R=R3 =CH3 ; R1 =R2 =C2H5), a white solid which melted at 217° to 218° C. A significant infrared maximum appeared at 1660 cm-1 (C=O;s). The nuclear magnetic resonance spectrum was consistent with the assigned structure. Paper coated with an ink formulation of the product produced a purple-colored image when contacted with an applied voltage stylus.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04549192
Source datasetuspto-grants-1985_10
ORD IDord-7d4cac4e96514b6db8f8776848abf179
Source noteuspto-grants-1985_10