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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 374514Generated: November 1, 2026

Hydrochloric Acid → 2-Thiopenecarboxaldehyde, 3,4,5-trichloro-

https://huagongshe.com/reaction/374514

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDimethylformamideHCID 6228—
Reactant2,3,4,5-TetrachlorothiopheneHCID 22344—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
SolventEthyl AcetateHCID 8857—
Product2-Thiopenecarboxaldehyde, 3,4,5-trichloro-HCID 15278484%

Reaction Conditions

Temperature0 °C

Reaction Steps

Butyllithium (2.5 molar in tetrahydrofuran, 3.96 mL, 9.9 mmol) is added to a solution of tetrachlorothiophene (2.00 g, 9.01 mmol) in tetrahydrofuran at 0° C. The reaction mixture is stirred at 0° C. for 30 minutes, warmed to room temperature over 45 minutes, treated with N,N-dimethylformamide (0.79 g, 10.8 mmol), stirred for three hours, poured into one molar hydrochloric acid at 4° C. and extracted with ether. The combined organic extracts are washed sequentially with water and brine, dried over MgSO4 and concentrated in vacuo to obtain a brown solid. Flash chromatography of the solid using silica gel and a 5% ethyl acetate in hexane solution gives a beige solid which is recrystallized from ethyl acetate and hexane to obtain the title product as beige needles (1.63 g, 84%, mp 81°-82° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05480902
Source datasetuspto-grants-1996_01
ORD IDord-5f224ebb82a945a08c08fe2453113b7d
Source noteuspto-grants-1996_01