HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 520798Generated: October 29, 2026
Dimethylformamide → Methyl 5-(chlorocarbonyl)thiophene-2-carboxylate
https://huagongshe.com/reaction/520798
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 69670373 | HCID 69670373 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | Methyl 5-(chlorocarbonyl)thiophene-2-carboxylate | HCID 21779986 | 371.2% |
Reaction Steps
150 g (749 mmol) of dimethyl thiophene-2,5-dicarboxylate in 1350 mL of toluene was azeotropically distilled at 130° C. to evaporate 150 mL of it. The reaction solution was cooled to an inner temperature of 70° C., then stirred with 300 mL of 2.5 M potassium hydroxide/methanol for 40 minutes and cooled to room temperature, and the precipitated solid was washed with ethyl acetate by filtration and dried under reduced pressure to obtain 160 g of potassium 5-(methoxycarbonyl)-thiophene-2-carboxylate. 100 g (446 mmol) of potassium 5-(methoxycarbonyl)-thiophene-2-carboxylate in 700 mL of 1,2-dichloroethane was mixed with 1.73 mL of N,N-dimethylformamide and heated to 90° C., and 68.9 g (119 mmol) of thionyl chloride was added dropwise. The reaction solution was refluxed for 1 hour and then cooled to room temperature, and the resulting crystals were filtered off with 300 mL of 1,2-dichloroethane. The filtrate was concentrated to dryness to obtain 90.4 g (yield 99%) of methyl 5-(chlorocarbonyl)thiophene-2-carboxylate (TEC).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09328085B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-4539422921e841acb5cf147a024bfff0 |
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| Source note | uspto-grants-2016_05 |
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