HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 235080Generated: October 30, 2026
Water → N,N-diethylthiophene-3-carboxamide
https://huagongshe.com/reaction/235080
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Thiophene-3-carboxylic acid | HCID 6918 | — |
| Reactant | Diethylamine | HCID 8021 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | N,N-diethylthiophene-3-carboxamide | HCID 11389776 | 88.7% |
Reaction Steps
A solution of 5.0 g (39 mmol) of 3-thiophenecarboxylic acid (Aldrich Chemical Co.), to which was added 10 mL (134 mmol) of SOCl2 in 20 mL of CHCl3 was stirred at reflux for 3 hours. After cooling to room temperature, the solution was concentrated in vacuo. The residue was dissolved in 15 mL of methylene chloride, and the solution was cooled in an ice bath. To this was added dropwise 13 mL (126 mmol) of diethyl amine, and the reaction was stirred at room temperature for 1 hour. Water was added, and the mixture was extracted with methylene chloride, which was washed with aqueous NaHCO3 solution, water, and bdne, and concentrated to give 9.3 g of crude product. This material was purified by flash chromatography on silica gel, eluting with 6:1 hexane:ethyl acetate, to afford 6.34 g of the title product after removal of the solvents. NMR (CDCl3) δ:7.48 (dd, 1H, J=1, J=3 Hz), 7.32 (dd, 1H, J=3, J=6 Hz), 7.20 (dd, 1H, J=1, J=6 Hz), 3.60-3.30 (bs, 4H), 1.20 (bm, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05597832 |
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| Source dataset | uspto-grants-1997_01 |
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| ORD ID | ord-01678aaaa51f4b0882703fad6e28a0cd |
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| Source note | uspto-grants-1997_01 |
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