benzyl 3-O-acetyl-2,4-di-O-benzyl-6-O-triphenylmethyl-α-D-glucopyranoside

Base Information

Chemical Name:benzyl 3-O-acetyl-2,4-di-O-benzyl-6-O-triphenylmethyl-α-D-glucopyranoside
CAS No.:77988-14-8
Molecular Formula:C₄₈H₄₆O₇
Molecular Weight:734.889
Hs Code.:

Synonyms:benzyl 3-O-acetyl-2,4-di-O-benzyl-6-O-triphenylmethyl-α-D-glucopyranoside

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of benzyl 3-O-acetyl-2,4-di-O-benzyl-6-O-triphenylmethyl-α-D-glucopyranoside

Chemical Property:

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Technology Process of benzyl 3-O-acetyl-2,4-di-O-benzyl-6-O-triphenylmethyl-α-D-glucopyranoside

There total 7 articles about benzyl 3-O-acetyl-2,4-di-O-benzyl-6-O-triphenylmethyl-α-D-glucopyranoside 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: 97.0%

: 108-24-7
acetic anhydride

: 40555-23-5
benzyl 2,4-di-O-benzyl-6-O-triphenylmethyl-α-D-glucopyranoside

: 77988-14-8
benzyl 3-O-acetyl-2,4-di-O-benzyl-6-O-triphenylmethyl-α-D-glucopyranoside

Guidance literature:: In pyridine;

Reference yield:

: 50-99-7
D-glucose

: 77988-14-8
benzyl 3-O-acetyl-2,4-di-O-benzyl-6-O-triphenylmethyl-α-D-glucopyranoside

Guidance literature:: Multi-step reaction with 4 steps

1: 36 percent / p-toluenesulfonic acid monohydrate / 4 h / 60 - 70 °C

2: 36 percent / pyridine / 3 h / 60 °C

3: 35 percent / potassium hydroxide / 2.5 h / 98 °C

4: 97 percent / pyridine

With potassium hydroxide; toluene-4-sulfonic acid; In pyridine;

Reference yield:

: 76-83-5
trityl chloride

: 77988-14-8
benzyl 3-O-acetyl-2,4-di-O-benzyl-6-O-triphenylmethyl-α-D-glucopyranoside

Guidance literature:: Multi-step reaction with 3 steps

1: 36 percent / pyridine / 3 h / 60 °C

2: 35 percent / potassium hydroxide / 2.5 h / 98 °C

3: 97 percent / pyridine

With potassium hydroxide; In pyridine;