HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1266933Generated: October 26, 2026
Formic Acid → 10-(4-Phenyl-2-thiazolylazo)-9-phenanthrol
https://huagongshe.com/reaction/1266933
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 9-Phenanthrol | HCID 10229 | — |
| Reactant | 2-Amino-4-phenylthiazole | HCID 40302 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 10-(4-Phenyl-2-thiazolylazo)-9-phenanthrol | HCID 135718516 | — |
Reaction Steps
A reaction flask was loaded with water (3.4 ml), a 98% aqueous solution of sulfuric acid (7.2 ml), 2-amino-4-phenylthiazol (1.66 g) and formic acid (1.6 ml) successively, followed by stirring to dissolve 2-amino-4-phenylthiazol. The liquid was cooled to 0° C., followed by dropwise addition of a solution in which sodium nitrite (0.47 g) was dissolved in water (2 ml) to the mixture in 10 minutes. After stirring at or below 5° C. for one hour, a solution in which 9-phenanthrol (3.2 g) was dissolved in ethanol (30 ml) was dropwise added to the mixture in one hour. The cooling was stopped and the reaction mixture at room temperature was filtrated to give crystals. The crystals were recrystallized with dioxane-methanol to give intended crystals (1.7 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06551682B1 |
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| Source dataset | uspto-grants-2003_04 |
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| ORD ID | ord-115edeb00daf4dcb951471066a214bf1 |
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| Source note | uspto-grants-2003_04 |
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