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67890-29-3

β-D-Glucopyranoside, phenylmethyl 2,3,4,6-tetrakis-O-(phenylmethyl)- synthesis

11synthesis methods
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Yield:67890-29-3 96%

Reaction Conditions:

with FeCl3/C in acetonitrile at 60; for 3 h;Mechanism;Inert atmosphere;Green chemistry;stereoselective reaction;Reagent/catalyst;Temperature;

Steps:

Reaction of 2,3,4,6-Tetra-O-benzyl-α-D-glucopyranoside with Alcohols and Phenols in the Presence of FeCl3/C; General Procedure

General procedure: A suspension of the FeCl3/C catalyst (2 mg, 0.002 mmol) in anhydCH3CN (6 mL) was prepared in a round-bottomed flask. A portion ofthis preparation (1.5 mL) was added to a mixture of required 2,3,4,6-tetra-O-benzyl-α-D-glucopyranoside (58 mg, 0.1 mmol) and the respective acceptor (0.12 mmol) in a round-bottomed flask (5 mL) under N2 atmosphere and the reaction mixture was stirred at 60 °C. After completion of the reaction (monitored by TLC), the organic phase was condensed under vacuum to obtain the crude product, whichwas purified by silica gel column chromatography (PE/EtOAc 40:1). All new compounds were fully characterized by 1H NMR, 13C NMR,and MS. Spectral and analytical data were in good agreement with the desired structures.

References:

Guo, Hong;Li, Juan;Si, Wenshuai;Tang, Jie;Tang, Tianjun;Wang, Zhongfu;Yang, Guofang;Zhang, Jianbo [Synthesis,2019,vol. 51,# 15,p. 2984 - 3000]