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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1431930Generated: November 2, 2026

Tetrahydrofuran → (S)-4-Benzyl-3-hexanoyl-2-oxazolidinone

https://huagongshe.com/reaction/1431930

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantHexaneHCID 8058—
Reactant(S)-4-Benzyl-2-oxazolidinoneHCID 736225—
ReactantButyllithiumHCID 178418339—
Product(S)-4-Benzyl-3-hexanoyl-2-oxazolidinoneHCID 10612452—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 4-(S)-benzyloxazolidin-2-one (56 mmol) (Aldrich, Milwaukee, Wis.) in THF at −78° C. is added 2.5 M n-BuLi in hexane (22:4 mL, 56 mmol) and the reaction is stirred at −78° C. for 2 hours. To this is added via cannula a −78° C. solution of acid chloride A-1 (R=hexanoyl, 65 mmol) in THF and the mixture is stirred at −78° C. for 2 hours, then allowed to warm to rt and stirred overnight. The reaction is then quenched with aqueous saturated NH4Cl, extracted with EtOAc, dried and purified by silica gel chromatography (hexanes/EtOAc) to afford N-hexanoyl-4-(S)-benzyloxazolidin-2-one (A-2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612059B2
Source datasetuspto-grants-2009_11
ORD IDord-c6061b08edd34edfa0b94a31768227b2
Source noteuspto-grants-2009_11