134660-05-2

Upstream product

• 572-09-8 2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromide 
• 2887-07-2 4-formylphenyl 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside 
• 123-08-0 4-hydroxy-benzaldehyde 
• 83-87-4 D-glucose pentaacetate 
• 203179-61-7 4-(tetra-O-acetyl-β-D-glucopyranosyloxy)-trans-cinnamaldehyde 

Downstream Products

• 120442-73-1 (E)-4-hydroxycinnamyl alcohol 4-O-β-D-glucopyranoside 

Relevant academic research and scientific papers

Coniferin and derivatives: A fast and easy synthesis via the aldehyde series using phase-transfer catalysis

Coniferin was synthesised in good yields (56% starting from vanillin) under mild conditions. A one-pot coupling of the glucosidation and Wittig- type reactions led to coniferaldehyde tetra-O-acetylglucoside, easily reduced into tetra-O-acetylconiferin by sodium borohydride. Similar procedures were used for the synthesis of syringin and the glucoside of 4-coumaryl alcohol.