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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 499725Erstellt: 25. Oktober 2026

Cyclohexane → HCID 78088908, Verbindung

https://huagongshe.com/reaction/499725

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCyclohexaneHCID 8078—
Edukt3,4,5-Tribenzyloxy-6-(benzyloxymethyl)tetrahydropyran-2-oneHCID 4585508—
Edukt2-Bromo-1,4-bis(trityloxymethyl)benzeneHCID 68458085—
EduktCID 53628100HCID 178418400—
LösungsmittelWaterHCID 962—
LösungsmittelTolueneHCID 1140—
ProduktHCID 78088908HCID 7808890880,1%

Reaktionsschritte

Under a nitrogen stream, to a solution of 2-bromo-1,4-bis(trityloxymethyl)benzene (255.3 mg, 0.36 mmol) in toluene (1.5 ml), a cyclohexane solution of sec-butyllithium (0.99 M, 367 μl, 0.36 mmol) was added dropwise at room temperature and the solution was stirred for 30 minutes. This solution was added dropwise at −78° C. to a solution of 3,4,5-trisbenzyloxy-6-(benzyloxymethyl)tetrahydropyran-2-one (140 mg, 0.26 mmol) in toluene (1.5 ml) and the mixture was stirred at the same temperature for 30 minutes. After addition of water, the reaction mixture was extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, and then evaporated under reduced pressure to remove the solvent. The resulting residue was purified by silica gel column chromatography (developing solution=ethyl acetate:n-hexane (1:5)) to give the titled compound (242 mg, 80%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07767651B2
Quelldatensatzuspto-grants-2010_08
ORD IDord-4fb96350c384456ebcf449f9b89690e7
Quellennotizuspto-grants-2010_08