2,2-dimethyl-propionic acid 3,4,5-triacetoxy-6-{7-acetylamino-6-[3,5-diacetoxy-2-allyloxy-6-(2,2-dimethyl-propionyloxymethyl)-tetrahydro-pyran-4-yloxy]-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-8-yloxy}-tetrahydro-pyran-2-ylmethyl ester

Base Information

• Chemical Name: 2,2-dimethyl-propionic acid 3,4,5-triacetoxy-6-{7-acetylamino-6-[3,5-diacetoxy-2-allyloxy-6-(2,2-dimethyl-propionyloxymethyl)-tetrahydro-pyran-4-yloxy]-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-8-yloxy}-tetrahydro-pyran-2-ylmethyl ester
• CAS No.: 253336-93-5
• Molecular Formula: C₅₀H₆₉NO₂₃
• Molecular Weight: 1052.09
• Mol file: 253336-93-5.mol

Synonyms:2,2-dimethyl-propionic acid 3,4,5-triacetoxy-6-{7-acetylamino-6-[3,5-diacetoxy-2-allyloxy-6-(2,2-dimethyl-propionyloxymethyl)-tetrahydro-pyran-4-yloxy]-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-8-yloxy}-tetrahydro-pyran-2-ylmethyl ester

Chemical Property of 2,2-dimethyl-propionic acid 3,4,5-triacetoxy-6-{7-acetylamino-6-[3,5-diacetoxy-2-allyloxy-6-(2,2-dimethyl-propionyloxymethyl)-tetrahydro-pyran-4-yloxy]-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-8-yloxy}-tetrahydro-pyran-2-ylmethyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 2,2-dimethyl-propionic acid 3,4,5-triacetoxy-6-{7-acetylamino-6-[3,5-diacetoxy-2-allyloxy-6-(2,2-dimethyl-propionyloxymethyl)-tetrahydro-pyran-4-yloxy]-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-8-yloxy}-tetrahydro-pyran-2-ylmethyl ester

There total 7 articles about 2,2-dimethyl-propionic acid 3,4,5-triacetoxy-6-{7-acetylamino-6-[3,5-diacetoxy-2-allyloxy-6-(2,2-dimethyl-propionyloxymethyl)-tetrahydro-pyran-4-yloxy]-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-8-yloxy}-tetrahydro-pyran-2-ylmethyl 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%

acetic anhydride (108-24-7) + 2,2-dimethyl-propionic acid 3,4,5-triacetoxy-6-{7-acetylamino-6-[2-allyloxy-6-(2,2-dimethyl-propionyloxymethyl)-3,5-dihydroxy-tetrahydro-pyran-4-yloxy]-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-8-yloxy}-tetrahydro-pyran-2-ylmethyl ester (253336-89-9) → 2,2-dimethyl-propionic acid 3,4,5-triacetoxy-6-{7-acetylamino-6-[3,5-diacetoxy-2-allyloxy-6-(2,2-dimethyl-propionyloxymethyl)-tetrahydro-pyran-4-yloxy]-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-8-yloxy}-tetrahydro-pyran-2-ylmethyl ester (253336-93-5)

Guidance literature:

With pyridine; dmap; at 20 ℃; for 12h;

DOI:10.1016/S0960-894X(99)00507-7

Reference yield:

benzaldehyde dimethyl acetal (1125-88-8) → 2,2-dimethyl-propionic acid 3,4,5-triacetoxy-6-{7-acetylamino-6-[3,5-diacetoxy-2-allyloxy-6-(2,2-dimethyl-propionyloxymethyl)-tetrahydro-pyran-4-yloxy]-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-8-yloxy}-tetrahydro-pyran-2-ylmethyl ester (253336-93-5)

Guidance literature:

Multi-step reaction with 3 steps

1: 85 percent / p-TsOH / acetonitrile / 0.67 h / 20 °C

2: 70 percent / Hg(CN)2; HgBr₂; MS 4A / 1,2-dichloro-ethane / 18 h / 40 - 45 °C

3: 95 percent / pyridine; DMAP / 12 h / 20 °C

With pyridine; dmap; mercury(II) cyanide; toluene-4-sulfonic acid; mercury dibromide; In 1,2-dichloro-ethane; acetonitrile; 1: transacetalization / 2: Condensation / 3: Acetylation;

DOI:10.1016/S0960-894X(99)00507-7

Reference yield:

2-methyl-(3,4,6-tri-O-acetyl-1,2-dideoxy-α-D-glucopyranoso)[1,2-d]-2-oxazoline (10378-06-0,20757-53-3,35954-65-5,123483-77-2,134308-33-1) → 2,2-dimethyl-propionic acid 3,4,5-triacetoxy-6-{7-acetylamino-6-[3,5-diacetoxy-2-allyloxy-6-(2,2-dimethyl-propionyloxymethyl)-tetrahydro-pyran-4-yloxy]-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-8-yloxy}-tetrahydro-pyran-2-ylmethyl ester (253336-93-5)

Guidance literature:

Multi-step reaction with 5 steps

1: 50 percent / BF₃*Et₂O; MS 4A / CH₂Cl₂ / 4 h / 20 °C

2: 90 percent / 1M MeONa/MeOH / CH₂Cl₂ / 0.33 h / -10 - -5 °C / pH 10

3: 85 percent / p-TsOH / acetonitrile / 0.67 h / 20 °C

4: 70 percent / Hg(CN)2; HgBr₂; MS 4A / 1,2-dichloro-ethane / 18 h / 40 - 45 °C

5: 95 percent / pyridine; DMAP / 12 h / 20 °C

With pyridine; methanol; dmap; boron trifluoride diethyl etherate; sodium methylate; mercury(II) cyanide; toluene-4-sulfonic acid; mercury dibromide; In dichloromethane; 1,2-dichloro-ethane; acetonitrile; 1: glycosylation / 2: Deacetylation / 3: transacetalization / 4: Condensation / 5: Acetylation;

DOI:10.1016/S0960-894X(99)00507-7

upstream raw materials:

acetic anhydride

2,2-dimethyl-propionic acid 3,4,5-triacetoxy-6-{7-acetylamino-6-[2-allyloxy-6-(2,2-dimethyl-propionyloxymethyl)-3,5-dihydroxy-tetrahydro-pyran-4-yloxy]-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-8-yloxy}-tetrahydro-pyran-2-ylmethyl ester

benzaldehyde dimethyl acetal

2-methyl-(3,4,6-tri-O-acetyl-1,2-dideoxy-α-D-glucopyranoso)[1,2-d]-2-oxazoline