HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2396534Generated: October 29, 2026
Hydrochloric Acid → 2-Thiopenecarboxaldehyde, 3,4,5-trichloro-
https://huagongshe.com/reaction/2396534
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Tetrachlorothiophene | HCID 22344 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-Thiopenecarboxaldehyde, 3,4,5-trichloro- | HCID 152784 | 84% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05492925 |
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| Source dataset | uspto-grants-1996_02 |
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| ORD ID | ord-1088ac0c7e4a42f6a48c6aa39dd10f62 |
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| Source note | uspto-grants-1996_02 |
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