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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 348395Generated: October 30, 2026

Hydrochloric Acid → HCID 60123706, compound

https://huagongshe.com/reaction/348395

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHCID 20741434HCID 20741434—
ReactantHCID 178418255HCID 178418255—
SolventTetrahydrofuranHCID 8028—
ProductHCID 60123706HCID 6012370689%

Reaction Steps

Under a nitrogen atmosphere, phenylmagnesium bromide (3N diethyl ether solution, 15 ml) was added dropwise to a tetrahydrofuran solution (50 ml) of N-methyl-N-methoxy-1-[1-(R)-phenylethyl]-5-oxopyrrolidine-3-(R)-carboxamide (2.49 g, 9.0 mmol), followed by stirring at room temperature for 30 minutes. To the reaction solution was added 1 mol/l hydrochloric acid (50 ml) under ice cooling and the mixture was extracted with ethyl acetate (8 ml×2). The organic layer was washed with saturated saline (100 ml) and dried over anhydrous sodium sulfate. After removal of the solvent under reduced pressure, the residue was subjected to silica gel column chromatography. Elution with n-hexane/ethyl acetate (1/1) afforded the title compound (2.36 g, 89%) as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176313B2
Source datasetuspto-grants-2007_02
ORD IDord-ac7b057d635b4ebc8cca86bf17b4bc4a
Source noteuspto-grants-2007_02