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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 81332Generated: October 25, 2026

aldehydo-D-Xylose → HCID 178478778, compound

https://huagongshe.com/reaction/81332

Reaction equation

Participants

RoleNameHCIDCharge
Reactantaldehydo-D-XyloseHCID 644160—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 178512152HCID 178512152—
SolventMethanolHCID 887—
ProductHCID 178478778HCID 17847877820.6%

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846688B2
Source datasetuspto-grants-2014_09
ORD IDord-eb41a332e2e24f28b2e765f175733482
Source noteuspto-grants-2014_09