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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1761365Generated: October 31, 2026

Hexane → HCID 11010755, compound

https://huagongshe.com/reaction/1761365

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantBenzenepropanoyl chlorideHCID 64801—
Reactant3-isopropyl-1,3-oxazolidin-2-oneHCID 237194—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11010755HCID 1101075582%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a stirred solution of 4 (2-propyl)-oxazo-lidine-2-one in anhydrous tetrahydrofuran (250 mL) under a nitrogen atmosphere at -78° C. were added in a dropwise fashion a solution of butyllithium in hexane (50 mL, 77.4 mmol) over 5 to 10 min. After stirring an additional 20 min at -78° C. 3-phenylpropionyl chloride (12.7 mL, 85.2 mmol) was added neat. The reaction was warmed to room temperature and stirred 1 to 2 h at the temperature. The reaction was quenched by adding 100 mL of saturated aqueous ammonium chloride and the volatiles removed by rotary evaporation. The resulting aqueous residue was extracted three times with ether and the combined organic phases were washed with brine, dried (Na2SO4), filtered and concentrated in vacuo. Recrystallization from hexanes/ethyl acetate provided the title compound (16.6 g, 82%). mp =86.5 to 87.5° C. Mass spectrum: (M+NH4)+ =279, (M+H)+=262. Mass spectrum: (M+NH4)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04826815
Source datasetuspto-grants-1989_05
ORD IDord-3aafd3891f8f45a09a21f8f4d806c63b
Source noteuspto-grants-1989_05