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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1160484Generated: October 30, 2026

Calcium diethanolate → E-3030 trihydrate

https://huagongshe.com/reaction/1160484

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCalcium diethanolateHCID 6451473—
ReactantBenzenepropanoic acid, 3-[(2S)-3-(4-chloro-2-cyanophenoxy)-2-fluoropropoxy]-α-(1-methylethoxy)-, (αS)-HCID 11949482—
SolventMethanolHCID 887—
ProductE-3030 trihydrateHCID 25033287141%

Reaction Steps

4.6 g of calcium diethoxide was dissolved in 500 mL of methanol, to which a methanol (300 mL) solution of 30.8 g of (2S)-3-[3-[(2S)-3-(4-chloro-2-cyanophenoxy)-2-fluoropropoxy]phenyl]-2-isopropoxypropionic acid was then added, followed by stirring the reaction mixture overnight at room temperature. Insoluble matter in the reaction mixture was filtered, and the solvent was distilled off under a reduced pressure. To the residue were added 250 mL of methanol and 60 mL of water, followed by heating the reaction mixture to reflux. The reaction mixture was then cooled, followed by filtering the precipitated solid to obtain 32 g of the title compound as a crude product. To this compound was added 1.5 L of ethanol, and the reaction mixture was heated to reflux. Insoluble matter was hot-filtered, and the solution was again heated to reflux. To the reaction mixture was added 20 ml of water to slowly cool the mixture, and the reaction mixture was stirred overnight at room temperature. The precipitated solid was filtered, washed with ethanol:water=9:1, and subjected to forced-air drying at 40° C. for 18 hours. There was obtained 29 g of the title compound in the form of white crystal. The 1H-NMR data thereof coincided with that of the compound of Example 1-(15).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07816405B2
Source datasetuspto-grants-2010_10
ORD IDord-62f28186de4a401f8c95649683efdd40
Source noteuspto-grants-2010_10