HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 854818Generated: October 30, 2026
2-Cyclopenten-1-one → HCID 14267878, compound
https://huagongshe.com/reaction/854818
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Cyclopenten-1-one | HCID 13588 | — |
| Reactant | Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1) | HCID 466102 | — |
| Reactant | (S,S)-(-)-HYDROBENZOIN | HCID 853020 | — |
| Solvent | Cyclohexane | HCID 8078 | — |
| Product | HCID 14267878 | HCID 14267878 | 676.8% |
Reaction Steps
A solution of (S,S)-hydrobenzoin (10.0 g, 46.7 mmol), pyridinium p-toluene sulfonate (1.4 g, 5.6 mmol), 2-cyclopentene-1-one (20 mL, 238.7 mmol) and cyclohexane (200 mL) was heated under reflux for 4 h with a Dean-Stark trap to remove water formed during the reaction. The mixture was then cooled in an ice bath for 20 min, and the insolubles were filtered off through filter aid. The resulting solution was washed with a 10% aqueous potassium bicarbonate solution (2×25 mL) and water (2×25 mL), and then dried over anhydrous sodium sulfate. The dried solution was passed through a pad of silica gel 60 (26 g of 230-400 mesh). The pad was further eluted with additional hexanes (475 mL). The resulting solution was concentrated in vacuo to afford 2(S),3(S)-diphenyl-1,4-dioxa-spiro[4.4]non-6-ene (10.55 g, 81%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07259166B2 |
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| Source dataset | uspto-grants-2007_08 |
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| ORD ID | ord-92b0cc5c8a804a28bee3b745afaefae5 |
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| Source note | uspto-grants-2007_08 |
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