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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 27233Generated: October 27, 2026

Potassium Iodide → Cyanomethyl 2-(cyanomethylthio)nicotinate

https://huagongshe.com/reaction/27233

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantSodium ChlorideHCID 5234—
ReactantDimethylformamideHCID 6228—
ReactantChloroacetonitrileHCID 7856—
ReactantPotassium BicarbonateHCID 516893—
ReactantHCID 178524460HCID 178524460—
SolventWaterHCID 962—
ProductCyanomethyl 2-(cyanomethylthio)nicotinateHCID 2532264—

Reaction Steps

12 Grams (0.16 mole) of chloroacetonitrile was added to a stirred suspension of 6.2 g (0.04 mole) of 2-mercaptonicotinic acid, 8.0 g (0.08 mole) of potassium bicarbonate, and 20 g (0.12 mole) of potassium iodide in 100 ml of dimethylformamide at 10° under nitrogen. The reaction was stirred at 10° for 7 hr., then at 25° for 15 hr. The reaction mixture was then poured into water, saturated with sodium chloride and filtered. The resulting solid was dissolved in methylene chloride, dried with magnesium sulfate and evaporated to give 7.5 g of cyanomethyl 2-(cyanomethylthio)nicotinate. m.p. 140°-143° C. NMR (DMSO) δ3.3(s,2); 4.3(s,2); 6.4(dd,1); 7.4(dd,1); 7.8(dd,1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04220776
Source datasetuspto-grants-1980_09
ORD IDord-db111377924643b9a7c91b19da1e9bd3
Source noteuspto-grants-1980_09