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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 229515Generated: October 30, 2026

Sodium Hydroxide → HCID 57758718, compound

https://huagongshe.com/reaction/229515

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantHCID 57758661HCID 57758661—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57758718HCID 57758718—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of the methyl 4-ethyl-3-methyl-5-oxo-1-[(R)-1-phenylethyl]pyrrolidin-3-yl-carboxylate (stereoisomer A) produced in Reference Example 32 (10.63 g, 36.7 mmol) in tetrahydrofuran (330 mL) and methanol (110 mL), 2N aqueous solution of sodium hydroxide (110 mL, 220 mmol) was added at room temperature, and the mixture was stirred in an oil bath at 60° C. for 5.5 hours. The reaction mixture was concentrated under reduced pressure, and after adding concentrated hydrochloric acid to the concentrate in an ice bath for acidification, the mixture was extracted with chloroform (300 mL+2×100 mL). The organic layers were combined, and dried with anhydrous sodium sulfate. After removing the dessicating agent by filtration, the solvent was removed by distillation under reduced pressure to obtain 11.46 g (quantitative) of the crude title compound as a pale brown solid. The crude product was used in the subsequent reaction with no further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07563805B2
Source datasetuspto-grants-2009_07
ORD IDord-75756df42da54bd3b2467a5bd2d7b62e
Source noteuspto-grants-2009_07