Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
Reactant1-chloro-2-(N-cyclopropylcarbamoyloxy)-2-ethoxyiminoethaneHCID 54380131—
ReactantPotassium 2-methylphenyl(4-bromophenyl)thionophosphinateHCID 131710027—
SolventMethyl Ethyl KetoneHCID 6569—
ProductO-[2-(N-cyclopropylcarbamoyloxy)-2-ethoxyiminoethyl] 2-methylphenyl(4-bromophenyl)thionophosphinateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03937824
Source datasetuspto-grants-1976_02
ORD IDord-830f603568f34fc589cc0d95b0dd9c6f
Source noteuspto-grants-1976_02