HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 66499Generated: October 25, 2026
Hydrochloric Acid → 3-(2-Thenoyl)propionic acid
https://huagongshe.com/reaction/66499
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Nitrobenzene | HCID 7416 | — |
| Reactant | Succinic anhydride | HCID 7922 | — |
| Reactant | Thiophene | HCID 8030 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Product | 3-(2-Thenoyl)propionic acid | HCID 78385 | 53% |
Reaction Steps
A solution of 0.3 mole of thiophene in 100 ml. of nitrobenzene is added dropwise with stirring to a cooled mixture of 30 g. (0.3 mole) of succinic anhydride, 87.8 g. (0.66 mole) of aluminum chloride and 300 ml. of nitrobenzene. The mixture is cooled and stirred for 30 minutes and then allowed to stand at room temperature overnight. The mixture is poured onto ice and 50 ml. of concentrated hydrochloric acid. The nitrobenzene is removed by steam distillation. The aqueous layer is decanted and the residue is mixed with 650 ml. of water and 20 g. of sodium carbonate. The mixture is heated, mixed with diatomaceous earth and filtered. The filtrate is acidified with concentrated hydrochloric acid and the solid which separates is filtered and washed with water. Recrystallization from water gives 53% of 4-oxo-4-(2-thienyl)butyric acid, m.p. 121°-123° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04342690 |
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| Source dataset | uspto-grants-1982_08 |
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| ORD ID | ord-1036f0ebc64e4301a2900110351aacae |
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| Source note | uspto-grants-1982_08 |
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