HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1995380Generated: November 2, 2026
Potassium Carbonate → O-ethyl O-(xanthen-9-one-4-yl) (2,4,6-trichlorophenyl)phosphonate
https://huagongshe.com/reaction/1995380
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Hydroxyxanthone | HCID 611428 | — |
| Reactant | O-Ethyl (2,4,6-trichlorophenyl)phosphonochloridate | HCID 53729853 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | O-ethyl O-(xanthen-9-one-4-yl) (2,4,6-trichlorophenyl)phosphonate | HCID 54313362 | — |
Reaction Steps
4-Hydroxyxanthen-9-one (0.01 mole), acetonitrile (25 ml) and potassium carbonate (0.01 mole) are charged into a glass reaction vessel fitted with a mechanical stirrer and thermometer. O-Ethyl (2,4,6-trichlorophenyl)phosphonochloridate (0.01 mole) in acetonitrile (6 ml) is added dropwise, with stirring, at room temperature. The reaction mixture is stirred for a period of about 48 hours at a temperature of from about 35° C. to 50° C. It is then cooled to room temperature and filtered. Solvent is stripped from the filtrate using a rotary evaporator (70° C., 15 mm Hg). The devolatilized residue is redissolved in 1/1 v/v chloroform/cyclohexane (25 ml). This solution is then slurried with silica gel (2 grams) at room temperature for a period of about 2 hours, then filtered. Solvent is stripped from the filtrate using a rotary evaporator to yield the desired product O-ethyl O-(xanthen-9-one-4-yl) (2,4,6-trichlorophenyl)phosphonate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04404220 |
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| Source dataset | uspto-grants-1983_09 |
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| ORD ID | ord-ea7b319e062744e88927e53131854903 |
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| Source note | uspto-grants-1983_09 |
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