Study on the preparation and hydrolysis of octa-O-benzyl sucrose was written by Jiao, Yan;Fang, Zhi-jie;Jiang, Rong-ying. And the article was included in Huaxue Shiji in 2007.Product Details of 126-14-7 This article mentions the following:
Sucrose octa-O-acetate was prepared by acetylation of sucrose, and then converted to octa-O-benzylsucrose was by benzylation with benzyl chloride in KOH. the overall product yield reached 81%. The octa-O-benzylsucrose was hydrolyzed to 2,3,4,6-tetra-O-benzyl glucose and 1,3,4,6-tetra-O-benzyl fructose using aqueous AcOH/H2SO4. In the experiment, the researchers used many compounds, for example, (2R,3R,4S,5R,6R)-2-(Acetoxymethyl)-6-(((2S,3S,4R,5R)-3,4-diacetoxy-2,5-bis(acetoxymethyl)tetrahydrofuran-2-yl)oxy)tetrahydro-2H-pyran-3,4,5-triyl triacetate (cas: 126-14-7Product Details of 126-14-7).
(2R,3R,4S,5R,6R)-2-(Acetoxymethyl)-6-(((2S,3S,4R,5R)-3,4-diacetoxy-2,5-bis(acetoxymethyl)tetrahydrofuran-2-yl)oxy)tetrahydro-2H-pyran-3,4,5-triyl triacetate (cas: 126-14-7) belongs to tetrahydrofuran derivatives. Tetrahydrofurans and furans are important oxygen-containing heterocycles that often exhibit interesting properties for biological applications or applications in the cosmetic industry. Commercial tetrahydrofuran contains substantial water that must be removed for sensitive operations, e.g. those involving organometallic compounds. Although tetrahydrofuran is traditionally dried by distillation from an aggressive desiccant, molecular sieves are superior.Product Details of 126-14-7
Referemce:
Tetrahydrofuran – Wikipedia,
Tetrahydrofuran | (CH2)3CH2O – PubChem