3,6-anhydro-1-O-benzyl-2,7,8-trideoxy-D-talo/galacto-oct-7-enitol

Base Information

• Chemical Name: 3,6-anhydro-1-O-benzyl-2,7,8-trideoxy-D-talo/galacto-oct-7-enitol
• CAS No.: 281666-21-5
• Molecular Formula: C₁₅H₂₀O₄
• Molecular Weight: 264.321
• Mol file: 281666-21-5.mol

Synonyms:3,6-anhydro-1-O-benzyl-2,7,8-trideoxy-D-talo/galacto-oct-7-enitol

Chemical Property of 3,6-anhydro-1-O-benzyl-2,7,8-trideoxy-D-talo/galacto-oct-7-enitol

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 3,6-anhydro-1-O-benzyl-2,7,8-trideoxy-D-talo/galacto-oct-7-enitol

There total 1 articles about 3,6-anhydro-1-O-benzyl-2,7,8-trideoxy-D-talo/galacto-oct-7-enitol which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 81.0%

3,6-anhydro-1-O-benzyl-2,7,8-trideoxy-4,5-O-isopropylidene-D-talo/galacto-oct-7-enitol (281666-28-2) → 3,6-anhydro-1-O-benzyl-2,7,8-trideoxy-D-talo/galacto-oct-7-enitol (281666-21-5)

Guidance literature:

With sulfuric acid; In 1,4-dioxane; for 3h; Heating;

DOI:10.1016/S0040-4020(00)00099-5

Reference yield: 84.0%

3,6-anhydro-1-O-benzyl-2,7,8-trideoxy-D-talo/galacto-oct-7-enitol (281666-21-5) → (3aR,6R,6aR)-5-(2-Benzyloxy-ethyl)-hexahydro-furo[3,2-b]furan-2,6-diol (281666-20-4)

Guidance literature:

With oxygen; copper(l) chloride; palladium dichloride; In water; N,N-dimethyl-formamide; at 20 ℃; for 24h;

DOI:10.1016/S0040-4020(00)00099-5

Reference yield:

3,6-anhydro-1-O-benzyl-2,7,8-trideoxy-D-talo/galacto-oct-7-enitol (281666-21-5) → (3aR,6aR)-2-(2-Benzyloxy-ethyl)-5-methoxy-hexahydro-furo[3,2-b]furan (281666-32-8)

Guidance literature:

Multi-step reaction with 4 steps

1: 84 percent / PdCl₂; CuCl; O₂ / dimethylformamide; H₂O / 24 h / 20 °C

2: 88 percent / HCl / 3 h / 20 °C

3: 92 percent / NaH / tetrahydrofuran / 1 h / 0 - 20 °C

4: 69 percent / n-Bu₃SnH; AIBN / toluene / 6 h / Heating

With hydrogenchloride; 2,2'-azobis(isobutyronitrile); oxygen; tri-n-butyl-tin hydride; sodium hydride; copper(l) chloride; palladium dichloride; In tetrahydrofuran; water; N,N-dimethyl-formamide; toluene; 1: Carbonylation / 2: Etherification / 3: Esterification / 4: Reduction;

DOI:10.1016/S0040-4020(00)00099-5

upstream raw materials:

3,6-anhydro-1-O-benzyl-2,7,8-trideoxy-4,5-O-isopropylidene-D-talo/galacto-oct-7-enitol

Downstream raw materials:

(3aR,6R,6aR)-5-(2-Benzyloxy-ethyl)-hexahydro-furo[3,2-b]furan-2,6-diol

(3aR,6aR)-2-(2-Benzyloxy-ethyl)-5-methoxy-hexahydro-furo[3,2-b]furan

(3R,3aR,6aR)-2-(2-Benzyloxy-ethyl)-5-methoxy-hexahydro-furo[3,2-b]furan-3-ol

dithiocarbonic acid O-[2-(2-benzyloxy-ethyl)-5-methoxy-hexahydro-furo[3,2-b]furan-3-yl] ester S-methyl ester