2-Nitro-benzoic acid (2R,3R,4R,5R,6S)-4-hydroxy-2-methoxy-6-methyl-5-((2S,3R,4S,5R,6R)-3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-3-yl ester

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Chemical Name:2-Nitro-benzoic acid (2R,3R,4R,5R,6S)-4-hydroxy-2-methoxy-6-methyl-5-((2S,3R,4S,5R,6R)-3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-3-yl ester
CAS No.:79258-21-2
Molecular Formula:C₂₈H₃₅NO₁₇
Molecular Weight:657.582
Hs Code.:

2-Nitro-benzoic acid (2R,3R,4R,5R,6S)-4-hydroxy-2-methoxy-6-methyl-5-((2S,3R,4S,5R,6R)-3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-3-yl ester

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Chemical Property of 2-Nitro-benzoic acid (2R,3R,4R,5R,6S)-4-hydroxy-2-methoxy-6-methyl-5-((2S,3R,4S,5R,6R)-3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-3-yl ester

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Technology Process of 2-Nitro-benzoic acid (2R,3R,4R,5R,6S)-4-hydroxy-2-methoxy-6-methyl-5-((2S,3R,4S,5R,6R)-3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-3-yl ester

There total 5 articles about 2-Nitro-benzoic acid (2R,3R,4R,5R,6S)-4-hydroxy-2-methoxy-6-methyl-5-((2S,3R,4S,5R,6R)-3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-3-yl 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:

: 79299-17-5
methyl endo/exo-2,3-O-(2-nitrobenzylidene)-α-L-rhamnopyranoside

: 79258-21-2
2-Nitro-benzoic acid (2R,3R,4R,5R,6S)-4-hydroxy-2-methoxy-6-methyl-5-((2S,3R,4S,5R,6R)-3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-3-yl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 85 percent / Hg(CN)2 / benzene; nitromethane

2: 1) 4percent HOAc, 2) CF₃COOOH / 1) MeOH, irradiation, 2) CH₂Cl₂, 0 deg C

With trifluoroacetyl peroxide; mercury(II) cyanide; acetic acid; In nitromethane; benzene;
DOI:10.1039/c39810000362

Reference yield:

: 572-09-8
2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromide

: 79258-21-2
2-Nitro-benzoic acid (2R,3R,4R,5R,6S)-4-hydroxy-2-methoxy-6-methyl-5-((2S,3R,4S,5R,6R)-3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-3-yl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 85 percent / Hg(CN)2 / benzene; nitromethane

2: 1) 4percent HOAc, 2) CF₃COOOH / 1) MeOH, irradiation, 2) CH₂Cl₂, 0 deg C

With trifluoroacetyl peroxide; mercury(II) cyanide; acetic acid; In nitromethane; benzene;
DOI:10.1039/c39810000362

Reference yield:

: 6919-96-6
2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromide

: 79258-21-2
2-Nitro-benzoic acid (2R,3R,4R,5R,6S)-4-hydroxy-2-methoxy-6-methyl-5-((2S,3R,4S,5R,6R)-3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-3-yl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 85 percent / mercury(II) cyanide / nitromethane; benzene / 24 h / 23 °C

2: 2.) trifluoroperacetic acid / 1.) acetic acid, methanol, irradiation, 45 min, 2.) dichloromethane, 0 deg C, 1.5 h

With trifluoroacetyl peroxide; mercury(II) cyanide; In nitromethane; benzene;