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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 550236Erstellt: 25. Oktober 2026

Ammonium Chloride → (3R,4S,5S,6R)-3,4,5-Trisbenzyloxy-6-benzyloxymethyl-2-[3-(5-fluorobenzo[b]thiophen-2-ylmethyl)naphthalen-1-yl]tetrahydropyran-2-ol

https://huagongshe.com/reaction/550236

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmonium ChlorideHCID 25517—
Edukt3,4,5-Tribenzyloxy-6-(benzyloxymethyl)tetrahydropyran-2-oneHCID 4585508—
Edukt2-(4-Bromonaphthalen-2-ylmethyl)-5-fluorobenzo[b]thiopheneHCID 67156577—
EduktHCID 178418244HCID 178418244—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(3R,4S,5S,6R)-3,4,5-Trisbenzyloxy-6-benzyloxymethyl-2-[3-(5-fluorobenzo[b]thiophen-2-ylmethyl)naphthalen-1-yl]tetrahydropyran-2-olHCID 6715743766%

Reaktionsschritte

In a nitrogen stream, an n-butyllithium hexane solution (1.6 M, 0.97 ml, 1.55 mmol) was added dropwise to a solution of 2-(4-bromonaphthalen-2-yl-methyl)-5-fluorobenzo[b]thiophene (520 mg, 1.41 mmol) in THF (15 ml) at −78° C. and the reaction mixture was stirred at the same temperature for 10 minutes. To this solution, a solution of 3,4,5-trisbenzyloxy-6-benzyloxymethyl-tetrahydropyran-2-one (835 mg, 1.55 mmol) in THF (3 ml) was added dropwise. The mixture was stirred at −78° C. for one hour, and a saturated ammonium chloride aqueous solution was added thereto to stop the reaction. The reaction mixture was extracted with ether, and the organic layer was washed with a saturated sodium chloride aqueous solution and dried (anhydrous magnesium sulfate), and then the solvent was distilled under reduced pressure. The obtained residue was purified by silica gel column chromatography [developing solution=ethyl acetate:n-hexane (1:20)] to obtain the title compound (770 mg, 66%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07943748B2
Quelldatensatzuspto-grants-2011_05
ORD IDord-e1fcc83317c5462b99a40d19af15ac35
Quellennotizuspto-grants-2011_05