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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1006741Generated: October 25, 2026

Resazurin → HCID 178515439, compound

https://huagongshe.com/reaction/1006741

Reaction equation

Participants

RoleNameHCIDCharge
ReactantResazurinHCID 11077—
CatalystZincHCID 23994—
SolventWaterHCID 962—
SolventAmmonium HydroxideHCID 14923—
ProductHCID 178515439HCID 178515439—

Reaction Steps

The crude resazurin compound was suspended in a mixture of 200 mL of water and 50 mL of conc. NH4OH. Zinc dust (2.0 g) was added and the suspension was stirred for 20 min. The resultant purple mixture was filtered, the filtrate was vigorously stirred on air to oxidize the leuco resorufin, the product of partial over reduction. The reaction was acidified with acetic acid, the brown solid formed was collected by filtration washed with water and dried. The yield was 2.1 g. The material contained ˜50% of 2,3,4-trihydro-2H-pyrano[3,2-b]phenoxazin-9-one, product of intramolecular cyclization which had been carried over from the first step. The rest of the material was the desired title compound 35.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06790945B2
Source datasetuspto-grants-2004_09
ORD IDord-e587c7737a6348ad902b1289b1fd2031
Source noteuspto-grants-2004_09