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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2308075Generated: October 31, 2026

Iodine → 2-Cyclopenten-1-one, 2-pentyl-

https://huagongshe.com/reaction/2308075

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantCyclopentanoneHCID 8452—
Reactant2-PentylidenecyclopentanoneHCID 86000—
Product2-Cyclopenten-1-one, 2-pentyl-HCID 11754984.3%

Reaction Steps

In a 100 ml four-neck flask fitted with a thermometer, a reflux condenser and a stirrer were placed 2-pentylidenecyclopentanone (30 g) synthesized in Reference Example 4, cyclopentanone (31.6 ml) and iodine (30 mg), followed by 4 hours of the reaction under refluxing. The reaction mixture was washed with water and the layers were separated from each other. The resulting organic layer was washed with saturated brine and separated. The organic layer was evaporated on a rotary evaporator under reduced pressure to recover cyclopentanone, whereby a crude product (30.2 g) was obtained. The product was distilled using a Claisen distillation apparatus to obtain 25.3 g of 2-pentyl-2-cyclopentenone (boiling point: 101° C./900 Pa; GC purity: 97.9%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06833481B2
Source datasetuspto-grants-2004_12
ORD IDord-995c1381a8524c619223a8a2f4350712
Source noteuspto-grants-2004_12