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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 854915Generated: October 30, 2026

Potassium Cyanide → ethyl 8-cyano-6-(trifluoromethoxy)-2-(trifluoromethyl)-2H-chromene-3-carboxylate

https://huagongshe.com/reaction/854915

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CyanideHCID 9032—
Reactantethyl 8-iodo-6-(trifluoromethoxy)-2-(trifluoromethyl)-2H-chromene-3-carboxylateHCID 86599457—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418397HCID 178418397—
SolventTetrahydrofuranHCID 8028—
SolventSodium chloride; waterHCID 57417360—
Productethyl 8-cyano-6-(trifluoromethoxy)-2-(trifluoromethyl)-2H-chromene-3-carboxylateHCID 8659946582%

Reaction Steps

A mixture of ethyl 8-iodo-6-(trifluoromethoxy)-2-(trifluoromethyl)-2H-chromene-3-carboxylate prepared as in Example 21a, Step 2 (2.00 g, 4.15 mmole), CuI (158 mg, 0.830 mmole), KCN (1.08 g, 16.6 mmole) and Pd(PPh3)4 (480 mg, 0.415 mmole) in anhydrous THF (5.0 mL) were refluxed under a dry N2 atmosphere for 2.5 days. The mixture was then poured into brine (100 mL), extracted with EtOAc (100 mL), dried over MgSO4 and concentrated in vacuo. Purification by silica chromatography followed by crystallization from EtOAc-hexanes gave 1.30 g (82% yield) of the product a yellow crystalline solid: EIHRMS m/z 399.0812 (M+NH4, C15H9NO4F6NH4, Calc'd 399.0774).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07259266B2
Source datasetuspto-grants-2007_08
ORD IDord-68ba58866bf441889605ac0f99e9631b
Source noteuspto-grants-2007_08