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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814498Generated: November 2, 2026

4-(1,3-Dioxolan-2-yl)benzonitrile → HCID 22502706, compound

https://huagongshe.com/reaction/1814498

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(1,3-Dioxolan-2-yl)benzonitrileHCID 2778428—
Reactantn-Methyl-2-methylthiophene-3-carboxamideHCID 22503091—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22502706HCID 2250270631.7%

Reaction Conditions

Temperature-70 °C

Reaction Steps

To a solution of N-methyl-2-methylthiophene-3-carboxamide (18.5 g) in tetrahydrofuran (350 ml) was dropwise added 2.5M n-butyl lithium (100 ml) at −70° C. The resulting solution was stirred at −70° C. for 1.5 hr, followed by the addition of a solution of 4-(1,3-dioxolan-2-yl)benzonitrile (20.9 g) in tetrahydrofuran (100 ml) at once. After the dry ice/acetone bath was removed, the reaction mixture was back to room temperature. Three hours later, an aqueous solution of saturated ammonium chloride was added thereto, and the organic layer was separated, washed with water and dried. The filtrate was concentrated, and the resulting solid was washed with ethyl acetate, tetrahydrofuran/ether and n-hexane in this order. The resulting solid was then dried, to give the title compound as white crystals (6.24 g, yield; 31.7%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06875761B2
Source datasetuspto-grants-2005_04
ORD IDord-ed283addf68e4cee800a57b569581b75
Source noteuspto-grants-2005_04