Participants
| Role | Name | HCID | Charge |
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| Reactant | NT2 purpurin | HCID 5487054 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 21H,22H-Porphine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05250668 |
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| Source dataset | uspto-grants-1993_10 |
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| ORD ID | ord-33480354086a4bdeb6738a7d455cca80 |
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| Source note | uspto-grants-1993_10 |
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