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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2243602Generated: October 29, 2026

2,3-Dihydroxybutanedioic Acid → 3-[5-(tert-Butyldimethylsilanyloxy)-5-(4-fluorophenyl)-1-(4-fluorophenylamino)-2-(2-oxo-4-phenyloxazolidine-3-carbonyl)pentyl]benzonitrile

https://huagongshe.com/reaction/2243602

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-Dihydroxybutanedioic AcidHCID 875—
ReactantChlorotrimethylsilaneHCID 6397—
ReactantDiisopropylethylamineHCID 81531—
Reactant3-[5-(tert-Butyldimethylsilanyloxy)-5-(4-fluorophenyl)pentanoyl]4-phenyloxazolidin-2-oneHCID 12111618—
Reactant3-[(4-Fluorophenylimino)methyl]benzonitrileHCID 22252051—
ReactantSodium BisulfiteHCID 23665763—
CatalystTitanium TetrachlorideHCID 24193—
SolventAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
Product3-[5-(tert-Butyldimethylsilanyloxy)-5-(4-fluorophenyl)-1-(4-fluorophenylamino)-2-(2-oxo-4-phenyloxazolidine-3-carbonyl)pentyl]benzonitrileHCID 22252068—

Reaction Conditions

Temperature-10 °C

Reaction Steps

At 10° C., 24 ml of diisopropylethylamine are added to 14 g of 3-[5-(tert-butyldimethyl-silanyloxy)-5-(4-fluorophenyl)pentanoyl]-4-phenyloxazolidin-2-one (10) and 12.5 g of 3-[(4-fluorophenylimino)methyl]benzonitrile 11 in 200 ml of methylene chloride, and 7.1 ml of trimethylsilyl chloride are added dropwise. After 1 h, 3.4 ml of titanium tetrachloride are added dropwise at −10° C. The mixture is stirred at −10° C. for 3 h and then allowed to stand at −30° C. for another 12 h. 8 ml of acetic acid and 140 ml of a 7% strength aqueous tartaric acid solution are then added, and stirring is continued at room temperature for another 2 h. 50 ml of 20% strength aqueous sodium hydrogen sulfite solution are added, and the mixture is then stirred for another hour and extracted with methylene chloride. The organic phase is dried over magnesium sulfate, concentrated and purified by silica gel chromatography (ethyl acetate/heptane=1/3→1/1). This gives 12

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07674773B2
Source datasetuspto-grants-2010_03
ORD IDord-25cb62ccce3140509b4a530c7997640a
Source noteuspto-grants-2010_03