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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1669474Generated: October 30, 2026

Hexane → HCID 10491506, compound

https://huagongshe.com/reaction/1669474

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
Reactant(S)-4-Benzyl-2-oxazolidinoneHCID 736225—
Reactant4-Pentenoyl chlorideHCID 4228493—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 10491506HCID 1049150672%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution (0.49 M) of (4S)-4-benzyl 1,3-oxazolidinone in THF cooled to −78° C. was added dropwise n-BuLi in hexane (2.5 M, 1.1 eq). The resulting solution was stirred at −78° C. for 30 min, then a solution of 4-pentenoyl chloride in THF (4 M, 1.1 eq) was added dropwise. The resulting mixture was stirred at −78° C. for 20 min and then allowed to reach 0° C., where it was stirred for another 40 min. The reaction was quenched by addition of sat. aq. NH4Cl before partitioning between H2O and EtOAc. The layers were separated and the aqueous phase re-extracted with EtOAc. The combined organic extracts were washed with brine, dried over Na2SO4, filtered and concentrated in vacuo. The residue was purified by FC eluting with PE/EtOAc (10:1) to give the product as a colourless oil (72%). (ES+) m/z 260 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07989438B2
Source datasetuspto-grants-2011_08
ORD IDord-cff3dffd2f8d4fb4a6db22762298f5da
Source noteuspto-grants-2011_08