HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1578595Generated: November 3, 2026
Potassium Iodide → O-[2-(N-cyclopropylcarbamoyloxy)-2-ethoxyiminoethyl] 2-methylphenyl(4-bromophenyl)thionophosphinate
https://huagongshe.com/reaction/1578595
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | 1-chloro-2-(N-cyclopropylcarbamoyloxy)-2-ethoxyiminoethane | HCID 54380131 | — |
| Reactant | Potassium 2-methylphenyl(4-bromophenyl)thionophosphinate | HCID 131710027 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | O-[2-(N-cyclopropylcarbamoyloxy)-2-ethoxyiminoethyl] 2-methylphenyl(4-bromophenyl)thionophosphinate | HCID 131710026 | — |
Reaction Steps
1-Chloro-2-(N-cyclopropylcarbamoyloxy)-2-ethoxyiminoethane (11 grams; 0.05 mole), methyl ethyl ketone (80 ml), potassium 2-methylphenyl(4-bromophenyl)thionophosphinate (17 grams; 0.05 mole) and a few crystals of potassium iodide are charged into a glass reaction flask equipped with a mechanical stirrer, thermometer and reflux condenser. The reaction mixture is then heated at reflux for a period of about 8 hours. After this time the reaction mixture is cooled to room temperature and is filtered to remove inorganic salts. The salts are washed with acetone and the washings combined with the filtrate. The resulting solution is stripped of solvents in a rotary evaporator. The remaining residue is dissolved in ether and the ether solution is washed with water and dried over anhydrous magnesium sulfate. The dried solution is filtered and stripped of ether to yield the desired product O-[2-(N-cyclopropylcarbamoyloxy)-2-ethoxyiminoethyl] 2-methylphenyl(4-bromophenyl)thionophosphinate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03937824 |
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| Source dataset | uspto-grants-1976_02 |
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| ORD ID | ord-830f603568f34fc589cc0d95b0dd9c6f |
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| Source note | uspto-grants-1976_02 |
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