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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1380826Generated: November 1, 2026

Sodium Iodide → O-ethyl S-(6-ethoxy-2-methyl-4-pyrimidinylmethyl) S-(n-propyl) dithiophosphate

https://huagongshe.com/reaction/1380826

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantHCID 23324656HCID 23324656—
Reactantpotassium O-ethyl S-(n-propyl) dithiophosphateHCID 23699411—
SolventAcetoneHCID 180—
ProductO-ethyl S-(6-ethoxy-2-methyl-4-pyrimidinylmethyl) S-(n-propyl) dithiophosphateHCID 57315843—

Reaction Conditions

Temperature45 °C

Reaction Steps

8.0 g (0.043 mol) of 6-ethoxy-4-chloromethyl-2-methyl-pyrimidine and 10.8 g (0.045 mol) of potassium O-ethyl S-(n-propyl) dithiophosphate are suspended in 20 ml of acetone. After the addition of a small amount (spatula tip) of sodium iodide the mixture is stirred well at 45° C. for 12 hours. The mixture is then filtered through Celite, the filtrate is concentrated under reduced pressure and the thus-isolated solid is taken up in 100 ml of toluene. The toluene solution is washed once with 5% sodium carbonate solution and once with saturated sodium chloride solution and dried over anhydrous sodium sulphate, and the solvent is removed by evaporation at 60° C. under reduced pressure. In this manner there is obtained O-ethyl S-(6-ethoxy-2-methyl-4-pyrimidinylmethyl) S-(n-propyl) dithiophosphate as an almost colourless oil, nD20 1.5385.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04584295
Source datasetuspto-grants-1986_04
ORD IDord-65aaff459f064f11b28e2bf9e069b82f
Source noteuspto-grants-1986_04