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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1275402Generated: October 30, 2026

Nonanoyl chloride → HCID 11834093, compound

https://huagongshe.com/reaction/1275402

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNonanoyl chlorideHCID 69819—
Reactant(S)-4-Benzyl-2-oxazolidinoneHCID 736225—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11834093HCID 1183409378%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 25.2 g (0.142 mol) of (S)-(-)-4-benzyl-2-oxazolidinone (Aldrich Chemical Company) in 300 mL of THF cooled to -78° C. was added 97.0 mL (0.155 mol) of 1.6M n-butyllithium. The reaction mixture was stirred at -78° C. for 1 hour and nonanoyl chloride (17.4 g, 0.129 mol), dissolved in 75 mL of THF, was then added. The resulting mixture was stirred at -78° C. for 3 hours and then quenched with 5% HCl solution. The resulting mixture was extracted with ether and the combined organics were washed with water, saturated sodium bicarbonate and brine. The organics were then dried over MgSO4, filtered and concentrated in vacuo. The residue was chromatographed on silica gel, eluting with ethyl acetate/hexanes (1:10), to provide 24.75 g (78%) of the desired product as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06160132
Source datasetuspto-grants-2000_12
ORD IDord-f900ce7d554b46e3b69a199956de98a7
Source noteuspto-grants-2000_12