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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1660464Generated: October 30, 2026

Potassium Hydroxide → alpha[m-(2-Phenyl-1,3-dioxa-2-cyclopentyl)phenyl]propionic acid

https://huagongshe.com/reaction/1660464

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantMethyl alpha-methylthio-alpha-[m-(2phenyl-1,3-dioxa-2-cyclopentyl)phenyl]propionateHCID 12819455—
CatalystZincHCID 23994—
CatalystCopper sulfate pentahydrateHCID 24463—
SolventWaterHCID 962—
Productalpha[m-(2-Phenyl-1,3-dioxa-2-cyclopentyl)phenyl]propionic acidHCID 12819457—

Reaction Steps

To 456 mg of methyl α-methylthio-α-(m-(2-phenyl-1,3-dioxa-2-cyclopentyl)phenyl)propionate were added 2.00 g of potassium hydroxide and 10 ml of water. The mixture was heated under reflux with stirring. A mixture of 100 mg of zinc powder and 10 mg of copper sulfate pentahydrate was added three times at 30 minute intervals, and the mixture was further heated under reflux for 24 hours with stirring. After cooling, 20 ml of water was added. The insoluble matter was separated by filtration, and washed with 20 ml of water. The filtrate and the washing were combined, and extracted with 10 ml of diethyl ether. The organic layer was adjusted to pH 1 with 3.5 ml of conc. hydrochloric acid, and extracted four times with 20 ml of diethyl ether. The organic layer was washed with 10 ml of water, and concentrated under reduced pressure to afford α-(m-(2-phenyl-1,3-dioxa-2-cyclopentyl)phenyl)propionic acid as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04308208
Source datasetuspto-grants-1981_12
ORD IDord-cf1f83a090544b55aee0d32a3f2f05b1
Source noteuspto-grants-1981_12