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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 854739Generated: October 30, 2026

Potassium Hydroxide → 2-(3-Chloro-4-methanesulfonyl-phenyl)-3-(tetrahydro-furan-3-yl)-propionic acid

https://huagongshe.com/reaction/854739

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 67190185HCID 67190185—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product2-(3-Chloro-4-methanesulfonyl-phenyl)-3-(tetrahydro-furan-3-yl)-propionic acidHCID 2195905794%

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of 2-(3-chloro-4-methanesulfonyl-phenyl)-3-(tetrahydro-furan-3-yl)-propionic acid methyl ester (729 mg, 2.10 mmol) in ethanol (20 mL) was treated with a solution of potassium hydroxide (694 mg, 10.51 mmol) in water (7 mL). The reaction was stirred for 3 h at 25° C., concentrated in vacuo to remove the ethanol, and then was acidified to pH=2 with a 1N aqueous hydrochloric acid solution. The resulting mixture was then extracted with methylene chloride 3×10 mL). The organic layers were dried over sodium sulfate, filtered, and concentrated in vacuo to afford 2-(3-chloro-4-methanesulfonyl-phenyl)-3-(tetrahydro-furan-3-yl)-propionic acid (654 mg, 94%) as a white foam: (ES)+-HRMS m/e calcd for C14H17ClO5S (M+Na)+ 355.0377. found 355.0382.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07259166B2
Source datasetuspto-grants-2007_08
ORD IDord-0aae88caee7d432e918d5a402becc731
Source noteuspto-grants-2007_08