HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1382858Generated: November 4, 2026
2-Thiophenecarboxaldehyde → HCID 785281, compound
https://huagongshe.com/reaction/1382858
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Thiophenecarboxaldehyde | HCID 7364 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 3-Benzoylpropionic acid | HCID 72871 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 785281 | HCID 785281 | — |
Reaction Steps
Thiophene-2-carboxaldehyde (27.4 cc), 3-benzoylpropionic acid (44.5 g), acetic anhydride (71 cc) and fused potassium acetate (20.5 g) are heated overnight at 80° C. The mixture is cooled to 40° C., chloroform is added and then poured onto crushed ice. Extraction is carried out with chloroform, the organic phase is washed with a decinormal sodium hydroxide solution, it is dried over magnesium sulfate and evaporated under reduced pressure. The residue is stirred for 45 minutes in 40°-60° petroleum spirit, filtered and dried. 5-Phenyl-3-(2-thienylmethylene)-2-furanone (45.3 g), m.p. 141° C., is thereby isolated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04808599 |
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| Source dataset | uspto-grants-1989_02 |
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| ORD ID | ord-573c30305e5f42898ed3363ad19c34d0 |
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| Source note | uspto-grants-1989_02 |
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