1,3,4-tri-O-acetyl-6-O-triphenylmethyl-2-desoxy-2-(p-methoxybenzylidene)amino-β-D-glucopyranose

Base Information

Chemical Name:1,3,4-tri-O-acetyl-6-O-triphenylmethyl-2-desoxy-2-(p-methoxybenzylidene)amino-β-D-glucopyranose
CAS No.:117991-55-6
Molecular Formula:C₃₉H₃₉NO₉
Molecular Weight:665.74
Hs Code.:

Synonyms:1,3,4-tri-O-acetyl-6-O-triphenylmethyl-2-desoxy-2-(p-methoxybenzylidene)amino-β-D-glucopyranose

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Chemical Property of 1,3,4-tri-O-acetyl-6-O-triphenylmethyl-2-desoxy-2-(p-methoxybenzylidene)amino-β-D-glucopyranose

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Technology Process of 1,3,4-tri-O-acetyl-6-O-triphenylmethyl-2-desoxy-2-(p-methoxybenzylidene)amino-β-D-glucopyranose

There total 5 articles about 1,3,4-tri-O-acetyl-6-O-triphenylmethyl-2-desoxy-2-(p-methoxybenzylidene)amino-β-D-glucopyranose 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:

: C₃₅H₃₅NO₇

: 108-24-7
acetic anhydride

: 117991-55-6
1,3,4-tri-O-acetyl-6-O-triphenylmethyl-2-desoxy-2-(p-methoxybenzylidene)amino-β-D-glucopyranose

Guidance literature:: at 25 ℃; for 24h; Inert atmosphere; Schlenk technique;
DOI:10.1016/j.carres.2013.09.006

Reference yield:

: 1078691-95-8
(+)-D-glucosamine hydrochloride

: 117991-55-6
1,3,4-tri-O-acetyl-6-O-triphenylmethyl-2-desoxy-2-(p-methoxybenzylidene)amino-β-D-glucopyranose

Guidance literature:: Multi-step reaction with 2 steps

1: 90 percent / 1N NaOH

2: 1.) pyridine / 1.) 3 d, r.t.; 2.) 24 h, r.t.

With pyridine; sodium hydroxide;

Reference yield:

: 123-11-5
4-methoxy-benzaldehyde

: 117991-55-6
1,3,4-tri-O-acetyl-6-O-triphenylmethyl-2-desoxy-2-(p-methoxybenzylidene)amino-β-D-glucopyranose

Guidance literature:: Multi-step reaction with 2 steps

1: 90 percent / 1N NaOH

2: 1.) pyridine / 1.) 3 d, r.t.; 2.) 24 h, r.t.

With pyridine; sodium hydroxide;