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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 81332Erstellt: 24. Oktober 2026

aldehydo-D-Xylose → HCID 178478778, Verbindung

https://huagongshe.com/de/reaction/81332

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktaldehydo-D-XyloseHCID 644160—
EduktSodium cyanoborohydrideHCID 5003444—
EduktHCID 178512152HCID 178512152—
LösungsmittelMethanolHCID 887—
ProduktHCID 178478778HCID 17847877820,6%

Reaktionsschritte

D-(+)-xylose (0.35 g, 2.6 mmol) was added to a solution of hydrochloride 4 (0.3 g, 0.65 mmol) in methanol (20 mL) and the mixture was stirred for 20 min at room temperature. Then the solution was cooled to −78° C. and sodium cyanoborohydride (0.17 g, 2.6 mmol) was added. The reaction mixture was stirred at −78° C. for 2 h and at room temperature for 4 d. After this time, the solvent was removed under reduced pressure and the residue was washed with water. The formed yellow solid was isolated and dried under vacuum. Then the residue was re-dissolved in 5% HCl and the solvent was removed at reduced pressure. The obtained compound was dissolved in water containing 0.1% TFA and purified by preparative HPLC (C 18 Luna column from Phenomenex 250×21.2 mm, 5μ, isocratic method, water/acetonitrile=80%:20%). The fractions containing the target compound were combined and the solvent was removed under reduced pressure. The residue was dissolved in 5% HCl and solvent was removed under reduced pressure (twice). The resulting yellow powder was dissolved in water and the solution was lyophylized to give 34 mg (7%) of compound 23 as a yellow solid. 1H NMR (300 MHz, CD3OD) δ 1.64 (br s., 4H), 2.62 (m, 2H), 3.30 (m, 4H), 3.35-3.70 (m, 13H), 4.23 (m, 2H), 4.47 (m, 2H), 6.95 (d, 2H), 7.15 (d, 2H). m/z (APCI)=689 [C28H45ClN8O10+H]+. [α]D25=−16.1° (c=0.5, MeOH).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08846688B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-eb41a332e2e24f28b2e765f175733482
Quellennotizuspto-grants-2014_09