3-O-(2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl)-1,2,4,5,6-penta-O-benzyl-sn-myoinositol

Base Information

• Chemical Name: 3-O-(2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl)-1,2,4,5,6-penta-O-benzyl-sn-myoinositol
• CAS No.: 93303-29-8
• Molecular Formula: C₇₅H₇₆O₁₁
• Molecular Weight: 1153.42

Synonyms:3-O-(2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl)-1,2,4,5,6-penta-O-benzyl-sn-myoinositol

Chemical Property of 3-O-(2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl)-1,2,4,5,6-penta-O-benzyl-sn-myoinositol

Chemical Property:

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Technology Process of 3-O-(2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl)-1,2,4,5,6-penta-O-benzyl-sn-myoinositol

There total 3 articles about 3-O-(2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl)-1,2,4,5,6-penta-O-benzyl-sn-myoinositol 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: 92.7%

benzyl chloride (100-44-7) + 1-O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-3,4,5,6-tetra-O-acetyl-sn-myo-inositol (29971-56-0,29971-57-1,29971-58-2,29971-59-3,130548-64-0,130548-65-1) → 1-O-(2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl)-2,3,4,5,6-penta-O-benzyl-sn-myo-inositol (93238-43-8,93303-29-8,93303-30-1,93303-31-2,121350-63-8)

Guidance literature:

With potassium hydroxide; at 100 ℃; for 12h;

Reference yield: 91.4%

benzyl chloride (100-44-7) + Acetic acid (2R,3S,4S,5R,6R)-4,5-diacetoxy-6-acetoxymethyl-2-((1S,2S,3R,4S,5R,6S)-2,3,4,5-tetrakis-benzyloxy-6-hydroxy-cyclohexyloxy)-tetrahydro-pyran-3-yl ester (62102-43-6,62138-02-7,62138-10-7,62138-11-8,62138-12-9,62138-13-0,64681-33-0) → 3-O-(2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl)-1,2,4,5,6-penta-O-benzyl-sn-myoinositol (93303-29-8)

Guidance literature:

With potassium hydroxide; at 100 ℃; for 6h;

Reference yield: 89.1%

benzyl chloride (100-44-7) + 3-O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-1,4,5,6-tetra-O-acetyl-sn-myo-inositol (29971-56-0,29971-57-1,29971-58-2,29971-59-3,130548-64-0,130548-65-1) → 3-O-(2,3,4,6-tetra-O-benzyl-α-D-mannopyranosyl)-1,2,4,5,6-penta-O-benzyl-sn-myo-inositol (93238-43-8,93303-29-8,93303-30-1,93303-31-2,121350-63-8)

Guidance literature:

With potassium hydroxide; at 100 ℃; for 12h;

upstream raw materials:

benzyl chloride

Acetic acid (2R,3S,4S,5R,6R)-4,5-diacetoxy-6-acetoxymethyl-2-((1S,2S,3R,4S,5R,6S)-2,3,4,5-tetrakis-benzyloxy-6-hydroxy-cyclohexyloxy)-tetrahydro-pyran-3-yl ester

1-O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-3,4,5,6-tetra-O-acetyl-sn-myo-inositol

3-O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-1,4,5,6-tetra-O-acetyl-sn-myo-inositol

Downstream raw materials:

(+)-2,3,4,5,6-pentakis-O-benzyl myo-inositol

1,2,4,5,6-penta-O-benzyl-sn-myo-inositol

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