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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2253965Generated: November 1, 2026

Lithium Hydroxide → (S)-2-Ethoxy-3-{2-[(5-methyl-2-phenyl-4-oxazolyl)methyl]benzofuran-5-yl}propanoic acid

https://huagongshe.com/reaction/2253965

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium HydroxideHCID 3939—
ReactantHCID 10530982HCID 10530982—
SolventTetrahydrofuranHCID 8028—
Product(S)-2-Ethoxy-3-{2-[(5-methyl-2-phenyl-4-oxazolyl)methyl]benzofuran-5-yl}propanoic acidHCID 10692663—

Reaction Conditions

Temperature0 °C

Reaction Steps

5-{(S)-2-Ethoxy-3-[(S)-4-benzyl-2-oxo-3-oxazolidinyl}-3-oxopropyl}-2-[(5-methyl-2-phenyl-4-oxazolyl)methyl]benzofuran (0.15 g, 0.26 mmol) was dissolved in tetrahydrofuran (5 ml). The solution was cooled to 0° C. and 0.5N lithium hydroxide (1.1 ml, 0.52 mmol) was added. After 15 minutes the bulk of the ethanol was removed, the residue was acidified with 1N HCl, diluted with water and extracted with ethyl acetate (3×). The combined extracts were washed with brine, dried over sodium sulfate and concentrated. The product was purified by flash-chromatography (hexanes/ethyl acetate/acetic acid, 10:10:1) then recrystallized from hexanes/ethyl acetate and obtained as a white solid (48 mg, mp 129° C., [α]D =-12.5° (c 0.99, CDCl3)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05232945
Source datasetuspto-grants-1993_08
ORD IDord-9fd949adbeaa4a189dd1700078b89a78
Source noteuspto-grants-1993_08