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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1899095Generated: November 1, 2026

Hydrochloric Acid → 5-(4-Fluorophenyl)-4-[4-(methylsulfonyl)phenyl]thiophene-2-carbaldehyde

https://huagongshe.com/reaction/1899095

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDimethylformamideHCID 6228—
Reactant2-(4-Fluorophenyl)-3-(4-methylsulfonylphenyl)thiopheneHCID 10336873—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product5-(4-Fluorophenyl)-4-[4-(methylsulfonyl)phenyl]thiophene-2-carbaldehydeHCID 23372717—

Reaction Steps

n-Butyl lithium (1.6M) in hexane (36 ml) was added dropwise to a stirred solution of 2-(4-fluorophenyl)-3-[4-(methylsulfonyl)phenyl]thiophene (8.0 g) in tetrahydrofuran (80 ml) at -60° C. The mixture was stirred for 30 minutes, and N,N-dimethylformamide (3.7 ml) was added dropwise over ten minutes to the mixture. The mixture was stirred at -70° to -20° C. for 2 hours. 1N Hydrochloric acid (70 ml) was added dropwise, and the solution was extracted with ethyl acetate. The extract was washed with brine, dried and concentrated. The residual syrup was purified by column chromatography on silica gel eluting with a mixture of toluene and ethyl acetate (9:1). The obtained crystals (4.5 g) were recrystallized from ethyl acetate to give pale yellow crystals of 5-(4-fluorophenyl)-4-[4-(methylsulfonyl)phenyl]thiophene-2-carbaldehyde (3.7 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05571810
Source datasetuspto-grants-1996_11
ORD IDord-21d2f5d7bd6344f9ac86c9e8e8a86324
Source noteuspto-grants-1996_11