HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 532598Generated: October 30, 2026
Hydrochloric Acid → HCID 86699213, compound
https://huagongshe.com/reaction/532598
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Benzoic acid, 3-fluoro-, ethyl ester | HCID 67975 | — |
| Reactant | 4H,5H,6H-cyclopenta[b]thiophen-4-one | HCID 1958632 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86699213 | HCID 86699213 | 14% |
Reaction Steps
5,6-Dihydro-cyclopenta[b]thiophen-4-one (2.1 g, 15.0 mmol) in 15 mL of THF was treated with NaH (60 percent, 1.5 g, 36 mmol). After the addition of 3-Fluoro-benzoic acid ethyl ester, 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 (70 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-(2-Fluoro-benzoyl)-5,6-dihydro-cyclopenta[b]thiophen-4-one (0.56 g, 2.1 mmol) as brown solid in 14% 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-125e1d60fc284ebd8954e782ab38a94f |
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| Source note | uspto-grants-2014_10 |
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