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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537966Generated: November 2, 2026

Methyl iodide → HCID 57544371, compound

https://huagongshe.com/reaction/537966

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium ethoxideHCID 2723922—
Reactant3-[3,5-Bis(trifluoromethyl)phenyl]-3-oxopropanenitrileHCID 24726815—
SolventEthanolHCID 702—
ProductHCID 57544371HCID 57544371—

Reaction Steps

A solution of sodium ethoxide (0.127 g, 1.87 mmol) in EtOH (5 mL) was treated with 3,5-bis(trifluoromethyl)benzoyl acetonitrile (0.500 g, 1.78 mmol) portionwise over 5 min. The reaction was heated at reflux for 30 min before the addition of methyl iodide (0.41 mL, 6.6 mmol). Heating at reflux was continued for a further 2 h before the reaction mixture was allowed to cool and concentrated in vacuo. The residue was partitioned between H2O (10 mL) and EtOAC (20 mL) and the aqueous phase was separated and re-extracted with EtOAC (2×20 mL). The combined organic extracts were washed with brine (25 mL), dried (MgSO4), filtered and concentrated. The crude product was purified by flash chromatography on silica gel (0-20% EtOAc in hexanes gradient) to afford 3-[3,5-bis(trifluoromethyl)phenyl]-2-methyl-3-oxopropanenitrile. 1H NMR (500 MHz, CDCl3) δ 8.21 (s, 2H), 8.10 (s, 1H), 4.42 (q, J=7.1 Hz, 1H), 1.71 (d, J=7.1 Hz, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08865707B2
Source datasetuspto-grants-2014_10
ORD IDord-7f589b786d3b4f268f241abe399fcfee
Source noteuspto-grants-2014_10