1-O-(2-O-benzoyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl) trichloroacetimidate

Base Information

• Chemical Name: 1-O-(2-O-benzoyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl) trichloroacetimidate
• CAS No.: 858525-76-5
• Molecular Formula: C₃₆H₃₄Cl₃NO₇
• Molecular Weight: 699.027
• Mol file: 858525-76-5.mol

Synonyms:1-O-(2-O-benzoyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl) trichloroacetimidate

Chemical Property of 1-O-(2-O-benzoyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl) trichloroacetimidate

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 1-O-(2-O-benzoyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl) trichloroacetimidate

There total 9 articles about 1-O-(2-O-benzoyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl) trichloroacetimidate 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: 91.0%

trichloroacetonitrile (545-06-2) + 2-O-benzoyl-3,4,6-tetra-O-benzyl-α-D-mannopyranoside (869213-53-6) → 1-O-(2-O-benzoyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl) trichloroacetimidate (858525-76-5)

Guidance literature:

With 1,8-diazabicyclo[5.4.0]undec-7-ene; In dichloromethane; at 0 ℃; for 1h; Inert atmosphere;

DOI:10.1002/chem.201304950

Reference yield:

2,3,4,6-Tetra-O-benzoyl-α-D-mannopyranosyl bromide (14218-11-2,14218-30-5,61198-88-7,108438-33-1,108836-02-8,114682-36-9,127305-34-4,151377-77-4) → 1-O-(2-O-benzoyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl) trichloroacetimidate (858525-76-5)

Guidance literature:

Multi-step reaction with 5 steps

1: 2,6-lutidine / CH₂Cl₂ / 72 h / 20 °C

2: 2.40 g / NaOMe / methanol / 24 h / 24 °C

3: 94 percent / imidazole; NaH / dimethylformamide / 2.5 h / 20 °C

4: acetic acid / H₂O / 2.5 h / 20 °C

5: 3.69 g / DBU / CH₂Cl₂ / 0.25 h / -5 °C

With 1H-imidazole; 2,6-dimethylpyridine; sodium methylate; sodium hydride; acetic acid; 1,8-diazabicyclo[5.4.0]undec-7-ene; In methanol; dichloromethane; water; N,N-dimethyl-formamide;

DOI:10.1021/jo061233x

Reference yield:

3,4,6-tri-O-benzyl-1,2-O-(α-methoxybenzylidene)-β-D-mannopyranose (915150-03-7) → 1-O-(2-O-benzoyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl) trichloroacetimidate (858525-76-5)

Guidance literature:

Multi-step reaction with 2 steps

1: acetic acid / H₂O / 2.5 h / 20 °C

2: 3.69 g / DBU / CH₂Cl₂ / 0.25 h / -5 °C

With acetic acid; 1,8-diazabicyclo[5.4.0]undec-7-ene; In dichloromethane; water;

DOI:10.1021/jo061233x

upstream raw materials:

trichloroacetonitrile

2-O-benzoyl-3,4,6-tetra-O-benzyl-α-D-mannopyranoside

2,3,4,6-Tetra-O-benzoyl-α-D-mannopyranosyl bromide

3,4,6-tri-O-benzyl-1,2-O-(α-methoxybenzylidene)-β-D-mannopyranose

Downstream raw materials:

2-O-benzoyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl-1-O-(1,2-O-isopropylidene-sn-glycerol)

1-O-allyl-2-O-(2-O-benzoyl-3,4,6-tri-O-benzyl-β-D-mannopyranosyl)-6-O-(2-O-benzoyl-3,4-di-O-benzyl-α-D-mannopyranosyl)-3,4,5-tri-O-benzyl-D-myo-inositol

1-O-allyl-2-O-(2-O-benzoyl-3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-6-O-(2-O-benzoyl-3,4-di-O-benzyl-α-D-mannopyranosyl)-3,4,5-tri-O-benzyl-D-myo-inositol