Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 20456899 | HCID 20456899 | — |
| Reactant | HCID 57251804 | HCID 57251804 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 56995103 | HCID 56995103 | — |
Reaction Steps
2-Hydroxy-4-trifluoromethylacridine (0.01 mole), triethylamine (0.01 mole), tetrahydrofuran (25 ml) are charged into a glass reaction vessel equipped with a mechanical stirrer and thermometer. The mixture is cooled to a temperature of about 0° C. and O-(4-nitrophenyl) S-ethyl phosphorochloridothioate (0.01 mole) dissolved in toluene (25 ml) is added with stirring over a period of about 30 minutes. After the addition is completed the reaction mixture is allowed to warm to room temperature and stirring is continued for a period of about 16 hours. After this time the reaction mixture is filtered to remove triethylamine hydrochloride. The filtrate is then washed with water, dried over anhydrous magnesium sulfate and stripped of solvents leaving a residue. This residue is subjected to flash chromatography using ethyl acetate as the eluant to yield the desired product O-(4-nitrophenyl) O-(4-trifluoromethylacridin-2-yl) S-ethyl phosphorothioate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04452792 |
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| Source dataset | uspto-grants-1984_06 |
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| ORD ID | ord-41f789cebd204ad3960ee5ee68d99c64 |
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| Source note | uspto-grants-1984_06 |
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