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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1021365Generated: October 25, 2026

Ethyl Acetate → HCID 67080394, compound

https://huagongshe.com/reaction/1021365

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantTrimethylsilyl cyanideHCID 82115—
Reactant7-fluoro-2,2-dimethyl-3,4-dihydro-2H-1-benzopyran-4-oneHCID 15205373—
Catalystzinc(II)iodideHCID 9883512—
SolventHydrochloric AcidHCID 313—
ProductHCID 67080394HCID 6708039424.25%

Reaction Conditions

Temperature50 °C

Reaction Steps

To 7-fluoro-2,2-dimethyl-2,3-dihydrochromen-4-one (1.000 g, 5.149 mmol) was added trimethylsilyl cyanide (3.215 mL, 25.75 mmol) followed by a spatula tip of zinc iodide. The reaction was heated at 50° C. for 1 hour. The reaction was cooled, diluted with ethyl acetate (40 mL) and washed with saturated sodium bicarbonate (2×25 mL), brine (25 mL), dried over magnesium sulfate and concentrated. The product was dissolved in 5 mL of acetic acid and 5 mL of HCl, and SnCl2 dihydrate (4.648 g, 20.60 mmol) was added. The reaction heated at reflux (130° C. oil bath temperature) overnight. The reaction was cooled, diluted with ethyl acetate (50 mL), washed with water (50 mL) and brine (50 mL), dried over magnesium sulfate and concentrated. The residue was purified by silica gel chromatography over silica gel eluting with a gradient of 0.5% MeOH/CH2Cl2 containing 0.5% acetic acid to 10% MeOH/CH2Cl2 containing 0.5% acetic acid to provide the title compound (0.280 g, 24.25% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716498B2
Source datasetuspto-grants-2014_05
ORD IDord-150d4e245b7741a38f0706ab981a186d
Source noteuspto-grants-2014_05