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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 373656Generated: October 30, 2026

Benzyl Alcohol → HCID 14213078, compound

https://huagongshe.com/reaction/373656

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantHexaneHCID 8058—
Reactant(4R)-3-((2R)-3-t-butoxycarbonyl-2-benzylpropionyl)-4-(2-propyl)-oxazolidine-2-oneHCID 14213076—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 14213078HCID 1421307894%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of dry benzyl alcohol (0.55 ml, 5.33 mmol) in anhydrous tetrahydrofuran (18 ml) under a nitrogen atmosphere at 0° C. was added a hexane solution of n-butyllithium (2.58 ml, 4.00 mmol). To this solution was added the product from Example 97 in anhydrous tetrahydrofuran (10 ml). After stirring 1 h at 0° C. the reaction was quenched by adding excess saturated aqueous ammonium chloride. The volatiles were removed by rotary evaporation and the resulting aqueous residue extracted two times with ether. The combined organic layers were washed with brine, dried (Na2SO4), filtered, and concentrated in vacuo provided an oil which was purified by chromatography on SiO2 (15% ether acetate/hexanes) to provide the desired product (0.89 g, 94%) as a colorless oil. Mass spectrum: (M)+ =354.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05164388
Source datasetuspto-grants-1992_11
ORD IDord-50e129011a79417393c1a29a8cfee3d3
Source noteuspto-grants-1992_11