ethyl 2-O-acetyl-6-O-tert-butyldiphenylsilyl-1-thio-β-D-galactopyranoside

Base Information

• Chemical Name: ethyl 2-O-acetyl-6-O-tert-butyldiphenylsilyl-1-thio-β-D-galactopyranoside
• CAS No.: 220281-18-5
• Molecular Formula: C₂₆H₃₆O₆SSi
• Molecular Weight: 504.72

Synonyms:ethyl 2-O-acetyl-6-O-tert-butyldiphenylsilyl-1-thio-β-D-galactopyranoside

Chemical Property of ethyl 2-O-acetyl-6-O-tert-butyldiphenylsilyl-1-thio-β-D-galactopyranoside

Chemical Property:

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Technology Process of ethyl 2-O-acetyl-6-O-tert-butyldiphenylsilyl-1-thio-β-D-galactopyranoside

There total 4 articles about ethyl 2-O-acetyl-6-O-tert-butyldiphenylsilyl-1-thio-β-D-galactopyranoside 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%

ethyl 2-O-acetyl-6-O-tert-butyldiphenylsilyl-3,4-O-isopropylidene-1-thio-β-D-galactopyranoside (220281-17-4) → ethyl 2-O-acetyl-6-O-tert-butyldiphenylsilyl-1-thio-β-D-galactopyranoside (220281-18-5)

Guidance literature:

With acetic acid; at 80 ℃; for 2h;

DOI:10.1081/SCC-120028645

Reference yield:

ethyl 3,4-O-isopropylidene-1-thio-β-D-galactopyranoside (172146-95-1) → ethyl 2-O-acetyl-6-O-tert-butyldiphenylsilyl-1-thio-β-D-galactopyranoside (220281-18-5)

Guidance literature:

Multi-step reaction with 3 steps

1: 78 percent / pyridine / 8 h / 25 °C

2: 94 percent / pyridine / 3 h / 20 °C

3: 91 percent / aq. acetic acid / 2 h / 80 °C

With pyridine; acetic acid;

DOI:10.1081/SCC-120028645

Reference yield:

tert-butylchlorodiphenylsilane (58479-61-1) → ethyl 2-O-acetyl-6-O-tert-butyldiphenylsilyl-1-thio-β-D-galactopyranoside (220281-18-5)

Guidance literature:

Multi-step reaction with 3 steps

1: 78 percent / pyridine / 8 h / 25 °C

2: 94 percent / pyridine / 3 h / 20 °C

3: 91 percent / aq. acetic acid / 2 h / 80 °C

With pyridine; acetic acid;

DOI:10.1081/SCC-120028645

upstream raw materials:

ethyl 2-O-acetyl-6-O-tert-butyldiphenylsilyl-3,4-O-isopropylidene-1-thio-β-D-galactopyranoside

tert-butylchlorodiphenylsilane

ethyl 3,4-O-isopropylidene-1-thio-β-D-galactopyranoside

ethyl 6‐O‐tert‐butyldiphenylsilyl‐3,4‐O‐isopropylidene‐1‐thio‐β‐D‐galactopyranoside

Downstream raw materials:

ethyl 2-O-acetyl-3-O-allyl-6-O-tert-butyldiphenylsilyl-1-thio-β-D-galactopyranoside

ethyl 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl-(1->3)-2-O-acetyl-4,6-O-benzylidene-1-thio-β-D-galactopyranoside

ethyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranosyl-(1->3)-2-O-acetyl-4,6-O-benzylidene-1-thio-β-D-galactopyranoside

ethyl 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl-(1->3)-2-O-acetyl-6-O-tert-butyldiphenylsilyl-1-thio-β-D-galactopyranoside

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