7103-29-9

Upstream product

• 50-70-4 D-sorbitol 

Downstream Products

• 135214-83-4 1,5-Anhydro-2-deoxy-4,6-O-(phenylmethylene)-D-arabino-hexopyranoside 
• 203862-58-2 1,5-anhydro-2-deoxy-4,6-O-p-methoxybenzylidene-D-arabino-hexitol 
• 13035-13-7 4,6-O-benzylidene-1,2-dideoxy-D-glucose 
• 171492-27-6 (3S,4R)-dihydroxy-(2R)-(triphenylmethoxymethyl)tetrahydropyran 
• 370887-48-2 (2R,3S,4S)-4-Benzyloxy-2-hydroxymethyl-tetrahydro-pyran-3-ol 
• 370886-63-8 ((2R,3R,4S)-4-Benzyloxy-2-prop-2-ynyl-tetrahydro-pyran-3-yloxy)-tert-butyl-dimethyl-silane 
• 370886-95-6 (2R,3R,4S)-4-Benzyloxy-3-(tert-butyl-dimethyl-silanyloxy)-2-(3-trimethylsilanyl-prop-2-ynyl)-tetrahydro-pyran 
• 370886-61-6 Trifluoro-methanesulfonic acid (2R,3S,4S)-4-benzyloxy-3-(tert-butyl-dimethyl-silanyloxy)-tetrahydro-pyran-2-ylmethyl ester 
• 370886-91-2 (2R,4aR,8S,8aS,2'R,4'S,4'aR,6'R,7'R,8'aR)-8,7'-Bis-benzyloxy-6'-benzyloxymethyl-4'-chloro-2-hydroxy-dodecahydro-[2,2']bi[pyrano[3,2-b]pyranyl]-3-one 
• 1054663-75-0 (2S,3S,4aR,8S,8aS,2'R,4'S,4'aR,6'R,7'R,8'aR)-8,7'-Bis-benzyloxy-6'-benzyloxymethyl-4'-chloro-dodecahydro-[2,2']bi[pyrano[3,2-b]pyranyl]-2,3-diol 
• 370886-89-8 {(2R,3R,4S)-4-Benzyloxy-2-[(Z)-3-((2R,4S,4aR,6R,7R,8aR)-7-benzyloxy-6-benzyloxymethyl-4-chloro-octahydro-pyrano[3,2-b]pyran-2-yl)-allyl]-tetrahydro-pyran-3-yloxy}-tert-butyl-dimethyl-silane 
• 1055028-95-9 (2R,4R,4aS,6R,7R,8aR)-7-Benzyloxy-2-{(Z)-3-[(2R,3R,4S)-4-benzyloxy-3-(tert-butyl-dimethyl-silanyloxy)-tetrahydro-pyran-2-yl]-propenyl}-6-benzyloxymethyl-octahydro-pyrano[3,2-b]pyran-4-ol 
• 1055029-63-4 1-((2R,4S,4aR,6R,7R,8aR)-7-Benzyloxy-6-benzyloxymethyl-4-chloro-octahydro-pyrano[3,2-b]pyran-2-yl)-3-[(2R,3S,4S)-4-benzyloxy-3-(tert-butyl-dimethyl-silanyloxy)-tetrahydro-pyran-2-yl]-propane-1,2-dione 
• 675834-58-9 1-((2R,4S,4aR,6R,7R,8aR)-7-Benzyloxy-6-benzyloxymethyl-4-chloro-octahydro-pyrano[3,2-b]pyran-2-yl)-3-[(2R,3S,4S)-4-benzyloxy-3-(tert-butyl-dimethyl-silanyloxy)-tetrahydro-pyran-2-yl]-propane-1,2-diol 

Relevant academic research and scientific papers

Effect of carbon chain length on catalytic C–O bond cleavage of polyols over Rh-ReOx/ZrO2 in aqueous phase

Production of linear deoxygenated C4 (butanetriols, -diols, and butanols), C5 (pentanetetraols, -triols, -diols, and pentanols), and C6 products (hexanepentaols, -tetraols, -triols, -diols, and hexanols) is achievable by hydrogenolysis of erythritol, xylitol, and sorbitol over supported-bimetallic Rh-ReOx (Re/Rh molar ratio 0.5) catalyst, respectively. After validation of the analytical methodology, the effect of some reaction parameters was studied. In addition to C–O bond cleavage by hydrogenolysis, these polyols can undergo parallel reactions such as epimerization, cyclic dehydration, and C–C bond cleavage. The time courses of each family of linear deoxygenated C4, C5, and C6 products confirmed that the sequence of appearance of the different categories of deoxygenated products followed a multiple sequential deoxygenation pathway. The highest selectivity to a mixture of linear deoxygenated C4, C5, and C6 products at 80percent conversion was favoured under high pressure in the presence of 3.7wt.percentRh-3.5wt.percentReOx/ZrO2 catalysts (54–71percent under 80 bar) at 200 °C.