methyl 3-O-benzyl-2-deoxy-2-C-methyl-6-O-trityl-α-D-altropyranoside

Base Information

• Chemical Name: methyl 3-O-benzyl-2-deoxy-2-C-methyl-6-O-trityl-α-D-altropyranoside
• CAS No.: 109914-91-2
• Molecular Formula: C₃₄H₃₆O₅
• Molecular Weight: 524.657
• Mol file: 109914-91-2.mol

Synonyms:methyl 3-O-benzyl-2-deoxy-2-C-methyl-6-O-trityl-α-D-altropyranoside

Chemical Property of methyl 3-O-benzyl-2-deoxy-2-C-methyl-6-O-trityl-α-D-altropyranoside

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of methyl 3-O-benzyl-2-deoxy-2-C-methyl-6-O-trityl-α-D-altropyranoside

There total 5 articles about methyl 3-O-benzyl-2-deoxy-2-C-methyl-6-O-trityl-α-D-altropyranoside 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%

trityl chloride (76-83-5) + methyl 3-O-benzyl-2-deoxy-2-C-methyl-α-D-altropyranoside (75837-45-5) → methyl 3-O-benzyl-2-deoxy-2-C-methyl-6-O-trityl-α-D-altropyranoside (109914-91-2)

Guidance literature:

In pyridine; at 70 ℃;

Reference yield:

methyl 2,3-anhydro-4,6-O-benzylidene-α-D-allopyranoside (2880-96-8,3150-15-0,3150-16-1,3257-59-8,14187-71-4,15384-57-3,19465-13-5,32976-15-1,52885-37-7,53270-02-3,53270-03-4,65391-11-9,65391-12-0,66537-92-6,67226-04-4,71184-14-0,86420-78-2,86420-79-3,91177-51-4,91177-52-5,117708-93-7,120408-72-2) → methyl 3-O-benzyl-2-deoxy-2-C-methyl-6-O-trityl-α-D-altropyranoside (109914-91-2)

Guidance literature:

Multi-step reaction with 4 steps

1: 56 percent / Cu(I)I / diethyl ether / 5 h / 0 °C

2: 94 percent / NaH / tetrahydrofuran / 18 h / Heating

3: 85 percent / toluene-p-sulphonic acid monohydrate / methanol / 3 h / 0 °C

4: 95 percent / pyridine / 70 °C

With copper(l) iodide; sodium hydride; toluene-4-sulfonic acid; In tetrahydrofuran; pyridine; methanol; diethyl ether;

Reference yield:

benzyl chloride (100-44-7) → methyl 3-O-benzyl-2-deoxy-2-C-methyl-6-O-trityl-α-D-altropyranoside (109914-91-2)

Guidance literature:

Multi-step reaction with 3 steps

1: 94 percent / NaH / tetrahydrofuran / 18 h / Heating

2: 85 percent / toluene-p-sulphonic acid monohydrate / methanol / 3 h / 0 °C

3: 95 percent / pyridine / 70 °C

With sodium hydride; toluene-4-sulfonic acid; In tetrahydrofuran; pyridine; methanol;

upstream raw materials:

trityl chloride

methyl 3-O-benzyl-2-deoxy-2-C-methyl-α-D-altropyranoside

benzyl chloride

methyl 3-O-benzyl-4,6-O-benzylidene-2-deoxy-2-C-methyl-α-D-altropyranoside

Downstream raw materials:

methyl 2,4-dideoxy-2,4-di-C-methyl-6-O-trityl-α-D-arabino-hexopyranosid-3-ulose

methyl 2,4-dideoxy-2,4-di-C-methyl-6-O-trityl-α-D-lyxopyranosid-3-ulose

methyl 2,4-dideoxy-2,4-di-C-methyl-6-O-trityl-α-D-altropyranoside

methyl 2,4-dideoxy-2,4-di-C-methyl-6-O-trityl-α-D-idopyranoside