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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1925893Generated: October 29, 2026

Lithium hydroxide, monohydrate → (S)-2-(8-methoxy-3-oxo-3,9-dihydro-1H-chromeno[2,3-c]pyrrol-2-yl)-3-cyclohexyl-propionic acid

https://huagongshe.com/reaction/1925893

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium hydroxide, monohydrateHCID 168937—
Reactant(S)-2-(8-methoxy-3-oxo-3,3a-dihydro-1H-chromeno[2,3-c]pyrrol-2-yl)-3-cyclohexyl-propionic acid methyl esterHCID 67520401—
SolventOxolane--water (1/1)HCID 21881883—
Product(S)-2-(8-methoxy-3-oxo-3,9-dihydro-1H-chromeno[2,3-c]pyrrol-2-yl)-3-cyclohexyl-propionic acidHCID 6752145995.7%

Reaction Steps

A solution of (S)-2-(8-methoxy-3-oxo-3,3a-dihydro-1H-chromeno[2,3-c]pyrrol-2-yl)-3-cyclohexyl-propionic acid methyl ester (1.2 g, 3.13 mmol) and lithium hydroxide monohydrate (0.17 g, 4.04 mmol) was stirred at 25° C. for 2 hours in tetrahydrofuran-water (3:1) mixture (20 mL). The reaction mixture was concentrated in vacuo to remove tetrahydrofuran, and the residue was acidified with 2N hydrochloric acid, and diluted with water. The resulting solution was extracted with ethyl acetate (3×). The combined organic layer was washed with brine and dried over anhydrous sodium sulfate. The solvent was removed in vacuo to afford (S)-2-(8-methoxy-3-oxo-3,9-dihydro-1H-chromeno[2,3-c]pyrrol-2-yl)-3-cyclohexyl-propionic acid (1.1 g, 95.7%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178689B2
Source datasetuspto-grants-2012_05
ORD IDord-ad847f121aa44aa2b10dfde88a1a15fa
Source noteuspto-grants-2012_05