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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2214109Generated: November 3, 2026

2-Cyclopenten-1-one → HCID 14267878, compound

https://huagongshe.com/reaction/2214109

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Cyclopenten-1-oneHCID 13588—
ReactantBenzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 466102—
Reactant(1S,2S)-1,2-diphenylethane-1,2-diolHCID 853020—
SolventCyclohexaneHCID 8078—
ProductHCID 14267878HCID 14267878676.8%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07105671B2
Source datasetuspto-grants-2006_09
ORD IDord-497a02f2e1304c5bb219081ac24d5421
Source noteuspto-grants-2006_09