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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1112709Generated: November 1, 2026

Acetone → 9-(3-Hydroxy-5-oxocyclopent-1-EN-1-YL)nonanoic acid

https://huagongshe.com/reaction/1112709

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantWaterHCID 962—
ReactantPotassium BromideHCID 253877—
Reactant4-Bromo-2-(8-carboxyoctyl)cyclopent-2-en-1-oneHCID 20465627—
CatalystSilver tetrafluoroborateHCID 159722—
SolventMethanolHCID 887—
Product9-(3-Hydroxy-5-oxocyclopent-1-EN-1-YL)nonanoic acidHCID 13289790—

Reaction Steps

To a stirred solution of 57.2 g. of crude 4-bromo-2-(8-carboxyoctyl)cyclopent-2-en-1-one (Example 1280) in 500 ml. of acetone and 325 ml. of water at 3° C. is added 44.1 g. (0.226 moles) of silver fluoborate during a 15 minute period. The mixture is stirred at 0°-3° C. for 2 hours and filtered. The filtrate is diluted with water, saturated with solid sodium chloride, and extracted with ether. The extract is washed with saturated sodium chloride solution, dried over magnesium sulfate, and concentrated. Partition chromatography of the residue on Celite gives white crystals, m.p. 58°-66° C., λmax.MeOH = 223 mμ (7800); νmax (KBr) = 3340 (hydroxyl groups), 1705 (carbonyl groups), and 1625 cm-1 (olefin group).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04123456
Source datasetuspto-grants-1978_10
ORD IDord-b1a85b4613224251aa38fc1475d6d103
Source noteuspto-grants-1978_10