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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1578601Generated: November 3, 2026

Potassium Iodide → HCID 131710031, compound

https://huagongshe.com/reaction/1578601

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantHCID 23720954HCID 23720954—
ReactantHCID 131710030HCID 131710030—
SolventMethyl Ethyl KetoneHCID 6569—
ProductHCID 131710031HCID 131710031—

Reaction Steps

1-Chloro-2-(N-3-allylphenylcarbamoyloxy)-2-methoxyiminoethane (14.1 grams; 0.05 mole), methyl ethyl ketone (100 ml), potassium 3-methylsulfinylphenyl(4-methylthiophenyl)phosphinate (18.2 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 6 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-3-allylphenylcarbamoyloxy)-2-methoxyiminoethyl] 3-methylsulfinylphenyl(4-methylthiophenyl)phosphinate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03937824
Source datasetuspto-grants-1976_02
ORD IDord-a7145957a3744b89afbd29c441814def
Source noteuspto-grants-1976_02