Acetic acid (2S,3S,4R,5S,6R)-3-acetoxy-6-[(S)-5-hydroxy-2-(4-hydroxy-phenyl)-4-oxo-chroman-7-yloxy]-2-methyl-5-((2S,3R,4R,5S,6S)-3,4,5-triacetoxy-6-methyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-4-yl ester

Base Information

Chemical Name:Acetic acid (2S,3S,4R,5S,6R)-3-acetoxy-6-[(S)-5-hydroxy-2-(4-hydroxy-phenyl)-4-oxo-chroman-7-yloxy]-2-methyl-5-((2S,3R,4R,5S,6S)-3,4,5-triacetoxy-6-methyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-4-yl ester
CAS No.:158694-45-2
Molecular Formula:C₃₇H₄₂O₁₈
Molecular Weight:774.73
Hs Code.:

Acetic acid (2S,3S,4R,5S,6R)-3-acetoxy-6-[(S)-5-hydroxy-2-(4-hydroxy-phenyl)-4-oxo-chroman-7-yloxy]-2-methyl-5-((2S,3R,4R,5S,6S)-3,4,5-triacetoxy-6-methyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-4-yl ester

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Chemical Property of Acetic acid (2S,3S,4R,5S,6R)-3-acetoxy-6-[(S)-5-hydroxy-2-(4-hydroxy-phenyl)-4-oxo-chroman-7-yloxy]-2-methyl-5-((2S,3R,4R,5S,6S)-3,4,5-triacetoxy-6-methyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-4-yl ester

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Technology Process of Acetic acid (2S,3S,4R,5S,6R)-3-acetoxy-6-[(S)-5-hydroxy-2-(4-hydroxy-phenyl)-4-oxo-chroman-7-yloxy]-2-methyl-5-((2S,3R,4R,5S,6S)-3,4,5-triacetoxy-6-methyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-4-yl ester

There total 1 articles about Acetic acid (2S,3S,4R,5S,6R)-3-acetoxy-6-[(S)-5-hydroxy-2-(4-hydroxy-phenyl)-4-oxo-chroman-7-yloxy]-2-methyl-5-((2S,3R,4R,5S,6S)-3,4,5-triacetoxy-6-methyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-4-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:

: 148081-37-2
3,4-di-O-acetyl-2-O-(2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl)-α-L-quinovopyranosyl bromide

: 480-41-1
naringenin

: 158694-45-2
Acetic acid (2S,3S,4R,5S,6R)-3-acetoxy-6-[(S)-5-hydroxy-2-(4-hydroxy-phenyl)-4-oxo-chroman-7-yloxy]-2-methyl-5-((2S,3R,4R,5S,6S)-3,4,5-triacetoxy-6-methyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-4-yl ester

Guidance literature:: With silver carbonate; In quinoline;
DOI:10.1271/bbb.58.1479

Reference yield:

: 158694-45-2
Acetic acid (2S,3S,4R,5S,6R)-3-acetoxy-6-[(S)-5-hydroxy-2-(4-hydroxy-phenyl)-4-oxo-chroman-7-yloxy]-2-methyl-5-((2S,3R,4R,5S,6S)-3,4,5-triacetoxy-6-methyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-4-yl ester

: 158694-63-4
naringenin 7-O-<2-O-(α-L-rhamnopyranosyl)-β-L-quinovopyranoside>

Guidance literature:: With sodium methylate; In methanol; at 0 ℃; for 2h; Yield given;
DOI:10.1271/bbb.58.1479

Reference yield:

: 158694-45-2
Acetic acid (2S,3S,4R,5S,6R)-3-acetoxy-6-[(S)-5-hydroxy-2-(4-hydroxy-phenyl)-4-oxo-chroman-7-yloxy]-2-methyl-5-((2S,3R,4R,5S,6S)-3,4,5-triacetoxy-6-methyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-4-yl ester

: naringenin dihydrochalcone 4'-O-<2-O-(α-L-rhamnopyranosyl)-β-L-quinovopyranoside>

Guidance literature:: Multi-step reaction with 2 steps

1: NaOCH₃ / methanol / 2 h / 0 °C

2: 94.5 percent / aq. KOH, H₂ / Pd/C / 3.5 h / Ambient temperature

With potassium hydroxide; hydrogen; sodium methylate; palladium on activated charcoal; In methanol;
DOI:10.1271/bbb.58.1479