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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1655445Generated: October 30, 2026

NT2 purpurin → 21H,22H-Porphine

https://huagongshe.com/reaction/1655445

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNT2 purpurinHCID 5487054—
SolventDichloromethaneHCID 6344—
Product21H,22H-PorphineHCID 137705241—

Reaction Steps

A 50 mg portion of Purpurin NT2 was dissolved in 20 ml dichloromethane, and the resulting solution was allowed to stand for a total of 16 hours in sunlight, in contact with air, and under ambient conditions (temperature about 22°). The dichloromethane was then removed by evaporation, leaving 50 mg porphyrin derivative (hereafter "Porphyrin NT2") which was found by nuclear magnetic resonance to have the formula of FIG. 9 of the attached drawings where R1 through R8 are ethyl, R10 through R12 are hydrogen, and R13 is CH2CH3. The production of Purpurin NT2 is described in Example 1 of PCT/US86/02824; it has the formula of FIG. 5 of the drawings of that application where R1 through R8 are ethyl, R9 is CO2CH2CH3, and R10 through R13 are hydrogen.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05250668
Source datasetuspto-grants-1993_10
ORD IDord-33480354086a4bdeb6738a7d455cca80
Source noteuspto-grants-1993_10