HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 532620Generated: October 31, 2026
Hydrochloric Acid → HCID 86699221, compound
https://huagongshe.com/reaction/532620
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ethyl Nicotinate | HCID 69188 | — |
| Reactant | 4H,5H,6H-cyclopenta[b]thiophen-4-one | HCID 1958632 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86699221 | HCID 86699221 | 55% |
Reaction Steps
5,6-Dihydro-cyclopenta[b]thiophen-4-one (1.66 g, 12 mmol) in 40 mL of THF was treated with NaH (60 percent, 2.4 g, 17 mmol). After the addition of Nicotinic acid ethyl ester (0.3 g, 20 mmol), the reaction mixture was heated at 100° C. for 8 hr. The solution was cooled to room temperature and poured into water. The resulting mixture was acidified with concentrated HCl and was added with ethyl acetate (80 mL). The organic layer was collected, brined, dried over MgSO4(s), and concentrated under reduced pressure. The resultant precipitate was collected and recrystallized from ethanol to provide the corresponding 5-(Pyridine-2-carbonyl)-5,6-dihydro-cyclopenta[b]thiophen-4-one (1.23 g, 8 mmol) as red solid in 55% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08853207B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-ee23fc66245c466ba82c1f6bbe7eb2f5 |
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| Source note | uspto-grants-2014_10 |
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