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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 18988Generated: October 27, 2026

Hydrochloric Acid → (S)-3-cyclohexyl-2-(4-methoxy-2-oxo-2,5-dihydro-pyrrol-1-yl)-propionic acid

https://huagongshe.com/reaction/18988

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantLithium hydroxide, monohydrateHCID 168937—
Reactant(S)-3-cyclohexyl-2-(4-methoxy-2-oxo-2,5-dihydro-pyrrol-1-yl)-propionic acid methyl esterHCID 66895604—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product(S)-3-cyclohexyl-2-(4-methoxy-2-oxo-2,5-dihydro-pyrrol-1-yl)-propionic acidHCID 6689465195.2%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution containing (S)-3-cyclohexyl-2-(4-methoxy-2-oxo-2,5-dihydro-pyrrol-1-yl)-propionic acid methyl ester (160 mg, 0.57 mmol) in tetrahydrofuran (3 mL) was treated with an aqueous solution of lithium hydroxide monohydrate (26 mg, 1.08 mmol) in water (3 mL). The mixture was stirred at 25° C. for 2.5 h. The mixture was then acidified with 2N aqueous hydrochloric acid. The mixture was extracted with dichloromethane (2×30 mL). The combined organic layers were dried over magnesium sulfate and concentrated. To afford (S)-3-cyclohexyl-2-(4-methoxy-2-oxo-2,5-dihydro-pyrrol-1-yl)-propionic acid (145 mg, 95%) as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741327B2
Source datasetuspto-grants-2010_06
ORD IDord-a8d4bc202f1842c88eea1fb230f352dc
Source noteuspto-grants-2010_06