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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1049569Generated: October 26, 2026

Isobutyronitrile → HCID 117760181, compound

https://huagongshe.com/reaction/1049569

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsobutyronitrileHCID 6559—
ReactantDiisopropylamineHCID 7912—
Reactant(E)-ethyl 3-(3-((methoxymethoxy)methyl)phenyl)acrylateHCID 131736029—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 117760181HCID 117760181—

Reaction Steps

Under a nitrogen atmosphere, a solution (1.6 M, 1.50 mL) of n-butyllithium in hexane was added to a solution of diisopropylamine (336 μL) in THF (2 mL) at −78° C., to the reaction mixture was added isobutyronitrile (227 μL) at −78° C., and the mixture was stirred for 5 min. To the reaction mixture was added (E)-ethyl 3-(3-((methoxymethoxy)methyl)phenyl)acrylate (250 mg) at −78° C., and the mixture was stirred at room temperature for 20 min. Water was added to the reaction mixture at room temperature, and the mixture was extracted with ethyl acetate. The extract was washed with water and saturated brine, and dried over anhydrous magnesium sulfate. The solvent of the reaction mixture was evaporated under reduced pressure and the residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (210 mg) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09382188B2
Source datasetuspto-grants-2016_07
ORD IDord-d1c7ee74a99a438fb6094020aa533cb5
Source noteuspto-grants-2016_07