Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1058651Generated: October 27, 2026

Hexane → 3-(4-Chlorobenzoyl)-2-(4-chlorophenylthio)-5-dimethoxymethylthiophene

https://huagongshe.com/reaction/1058651

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
Reactant4-Chloro-N-methoxy-N-methylbenzamideHCID 11275663—
Reactant3-Bromo-2-(4-chlorophenylthio)-5-dimethoxymethylthiopheneHCID 18668927—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product3-(4-Chlorobenzoyl)-2-(4-chlorophenylthio)-5-dimethoxymethylthiopheneHCID 1866900960%

Reaction Steps

In an argon atmosphere, 3-bromo-2-(4-chlorophenylthio)-5-dimethoxymethylthiophene (500 mg, 1.32 mmol) obtained in Example 90 was dissolved in tetrahydrofuran (6 mL) and cooled to −78° C. n-Butyl lithium (a 1.6 mol/L hexane solution, 0.81 mL, 1.3 mmol) and tetrahydrofuran (1 mL) solution of 4-chloro-N-methoxy-N-methylbenzamide (528 mg, 2.64 mmol) were added thereto, followed by stirring for 10 minutes. Water was added to the reaction liquid and the product was extracted with ethyl acetate. The organic layer was washed with water and brine, and then dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (15:1 hexane/ethyl acetate) to give 3-(4-chlorobenzoyl)-2-(4-chlorophenylthio)-5-dimethoxymethylthiophene (345 mg, 60%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06518268B1
Source datasetuspto-grants-2003_02
ORD IDord-8bf48d9fca4f4237899c4e137fe698a0
Source noteuspto-grants-2003_02