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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1071627Generated: November 3, 2026

Dimethylformamide → 3-(1,3-dioxolan-2-yl)thiophene-2-carbaldehyde

https://huagongshe.com/reaction/1071627

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-(3-Thienyl)-1,3-dioxolaneHCID 315630—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product3-(1,3-dioxolan-2-yl)thiophene-2-carbaldehydeHCID 1150657262.5%

Reaction Conditions

Temperature-70 °C

Reaction Steps

5.00 g (32.0 mmol) of 3-(1,3-dioxolan-2-yl)thiophene was dissolved in 100 ml of THF. 24.5 ml (1.5 mol/l) of n-butyllithium was added dropwise thereinto. After stirring for 0.5 hour, the mixture was cooled to −70° C., 3.10 ml (40.0 mmol) of DMF was added, and then the mixture was transferred to an ice bath. After stirring for about 2 hours, an aqueous saturated ammonium chloride was added, and the mixture was extracted with ethyl acetate. The extract was washed with brine, and then dried over anhydrous magnesium sulfate. The solvent was evaporated, to give a crude product. The crude product was subjected to silica gel (ethyl acetate:hexane=1:2), to give 3.68 g (20.0 mmol, 62.4%) of the title compound as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06906072B1
Source datasetuspto-grants-2005_06
ORD IDord-1d443a390ba649ef88ae65cb63f68d26
Source noteuspto-grants-2005_06