920015-39-0

Basic information

• Product Name: 6-O-trityl-D-galactono-1,4-lactone
• Synonyms: 6-O-trityl-D-galactono-1,4-lactone
• CAS NO: 920015-39-0
• Molecular Weight: 420.462
• Mol File: 920015-39-0.mol

Chemical Properties

• CAS DataBase Reference: 6-O-trityl-D-galactono-1,4-lactone(CAS DataBase Reference)
• NIST Chemistry Reference: 6-O-trityl-D-galactono-1,4-lactone(920015-39-0)
• EPA Substance Registry System: 6-O-trityl-D-galactono-1,4-lactone(920015-39-0)

Safety Data

• Hazardous Substances Data: 920015-39-0(Hazardous Substances Data)

Upstream product

• 76-83-5 trityl chloride 
• 2782-07-2 D-galactono-1,4-lactone 

Downstream Products

• 104826-50-8 2,3,5-tri-O-benzoyl-6-O-trityl-D-galactono-1,4-lactone 
• 123765-15-1 2,3,5-tri-O-benzoyl-D-galactono-1,4-lactone 
• 123783-57-3 2,3,5-tri-O-benzoyl-6-O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-D-galactono-1,4-lactone 
• 123765-17-3 2,3,5-tri-O-benzoyl-6-O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-β-D-galactofuranose 
• 123765-16-2 3,4,6-tri-O-acetyl-1,2-O-<1(S)-(2,3,5-tri-O-benzoyl-D-galactono-1,4-lactone-6-yloxy)ethylidene>-α-D-glucopyranose 
• 76-84-6 triphenylmethyl alcohol 

Relevant articles and documents

Facile synthesis of a d-galactono-1,6-lactone derivative, a precursor of a copolyester

2,3,4,6-Tetra-O-methyl-d-galactonic acid (5) was readily prepared from d-galactono-1,4-lactone (1) in 47% yield. The sequence involves tritylation of HO-6 of 1, followed by O-permethylation and deprotection. Lactonization of 5 led to the per-O-methyl-d-ga

A NEW APPROACH TO THE SYNTHESIS OF DISACCHARIDE DERIVATIVES HAVING A FURANOSE AS THE REDUCING UNIT

The lactonic disaccharide 2,3,5-tri-O-benzoyl-6-O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-D-galactono-1,4-lactone (7) was prepared by condensing 6-O-trityl-2,3,5-tri-O-benzoyl-D-galactono-1,4-lactone (2) with 2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromide (4) or with 1,2,3,4,6-penta-O-acetyl-β-D-glucopyranose (6).The reaction was carried out using various catalysts.In the presence of silver trifluoromethanesulfonate or tin(IV) chloride, formation of the 1,2-trans glycosidic bond took place stereoselectively, to afford compound 7 in good yields.However, condensation of 2,3,5-tri-O-benzoyl-D-galactono-1,4-lactone (3) with 4 catalyzed by mercuric salts gave 3,4,6-tri-O-acetyl-1,2-O--α-D-glucopyranose (5) as the main product.Reduction of the lactone function of 7 with bis(3-methyl-2-butyl)borane led to 2,3,5-tri-O-benzoyl-6-O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-β-D-galactofuranose (8).