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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 334390Generated: October 30, 2026

Iodine → HCID 178503563, compound

https://huagongshe.com/reaction/334390

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantHCID 178503531HCID 178503531—
CatalystHCID 178418844HCID 178418844—
SolventEthanolHCID 702—
ProductHCID 178503563HCID 17850356390.7%

Reaction Steps

6 g (1.6 eq) of silver sulfate and 4.58 g (1.5 eq) of iodine are added successively to a solution of 2 g (12 mmol) of 6-hydroxy-2-(methylthio)nicotinonitrile in 200 ml of ethanol. The reaction medium is stirred at room temperature for 2 hours. The solid is filtered and the residue rinsed thoroughly with methanol. The filtrate is evaporated and then taken up in ethyl acetate. The organic phase is washed with water three times, dried on magnesium sulfate and evaporated to yield 3.18 g (90%) of 6-hydroxy-5-iodo-2-(methylthio)nicotinonitrile in the form of a yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883821B2
Source datasetuspto-grants-2014_11
ORD IDord-b21d125b123c4dc3a63d9ecc748874b6
Source noteuspto-grants-2014_11