Acetic acid (1S,2R,3S,4R,5R,6R)-3,4-dihydroxy-2,5,6-tris-phosphonooxy-cyclohexyl ester

Base Information

Chemical Name:Acetic acid (1S,2R,3S,4R,5R,6R)-3,4-dihydroxy-2,5,6-tris-phosphonooxy-cyclohexyl ester
CAS No.:178152-66-4
Molecular Formula:C₈H₁₇O₁₆P₃
Molecular Weight:462.135
Hs Code.:

Synonyms:Acetic acid (1S,2R,3S,4R,5R,6R)-3,4-dihydroxy-2,5,6-tris-phosphonooxy-cyclohexyl ester

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Chemical Property of Acetic acid (1S,2R,3S,4R,5R,6R)-3,4-dihydroxy-2,5,6-tris-phosphonooxy-cyclohexyl ester

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Technology Process of Acetic acid (1S,2R,3S,4R,5R,6R)-3,4-dihydroxy-2,5,6-tris-phosphonooxy-cyclohexyl ester

There total 3 articles about Acetic acid (1S,2R,3S,4R,5R,6R)-3,4-dihydroxy-2,5,6-tris-phosphonooxy-cyclohexyl ester 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: 95.0%

: 5-O-Acetyl-2,3-O-cyclohexylidene-myo-inositol 1,4,6-tris(dibenzylphosphate)

: 178152-66-4
Acetic acid (1S,2R,3S,4R,5R,6R)-3,4-dihydroxy-2,5,6-tris-phosphonooxy-cyclohexyl ester

Guidance literature:: With hydrogen; palladium on activated charcoal; In acetic acid; for 3h; Ambient temperature;

Reference yield:

: 6763-47-9,1251832-23-1
rac-1,2-O-cyclohexylidene-myo-inositol

: 178152-66-4
Acetic acid (1S,2R,3S,4R,5R,6R)-3,4-dihydroxy-2,5,6-tris-phosphonooxy-cyclohexyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: pyridine, 3 Angstroem and 4 Angstroem molecular sieves / toluene / 96 h / Ambient temperature; porcine pancreatic lipase

2: 1H-tetrazole / acetonitrile / 2 h / Ambient temperature

3: 30percent CH₃CO₃H / acetonitrile

4: 95 percent / H₂ / 10percent Pd/C / acetic acid / 3 h / Ambient temperature

With pyridine; 1H-tetrazole; peracetic acid; molecular sieve; hydrogen; palladium on activated charcoal; In acetic acid; toluene; acetonitrile;

Reference yield:

: 1L-5-O-acetyl-1,2-O-cyclohexylidene-myo-inositol

: 178152-66-4
Acetic acid (1S,2R,3S,4R,5R,6R)-3,4-dihydroxy-2,5,6-tris-phosphonooxy-cyclohexyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 1H-tetrazole / acetonitrile / 2 h / Ambient temperature

2: 30percent CH₃CO₃H / acetonitrile

3: 95 percent / H₂ / 10percent Pd/C / acetic acid / 3 h / Ambient temperature

With 1H-tetrazole; peracetic acid; hydrogen; palladium on activated charcoal; In acetic acid; acetonitrile;