2-(4-(2-chloro-5-((2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)benzyl)phenoxy)acetaldehyde O-methyl oxime

Base Information

Chemical Name:2-(4-(2-chloro-5-((2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)benzyl)phenoxy)acetaldehyde O-methyl oxime
CAS No.:1426924-84-6
Molecular Formula:C₂₂H₂₆ClNO₇
Molecular Weight:451.904
Hs Code.:

Synonyms:2-(4-(2-chloro-5-((2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)benzyl)phenoxy)acetaldehyde O-methyl oxime

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Chemical Property of 2-(4-(2-chloro-5-((2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)benzyl)phenoxy)acetaldehyde O-methyl oxime

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Technology Process of 2-(4-(2-chloro-5-((2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)benzyl)phenoxy)acetaldehyde O-methyl oxime

There total 12 articles about 2-(4-(2-chloro-5-((2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)benzyl)phenoxy)acetaldehyde O-methyl oxime 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: 96.2%

: 1426924-86-8
(2R,3R,4R,5S,6S)-2-(acetoxymethyl)-6-(4-chloro-3-(4-(2-(methoxyimino)ethoxy)benzyl)phenyl)tetrahydro-2H-pyran-3,4,5-triyl triacetate

: 1426924-84-6
2-(4-(2-chloro-5-((2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)benzyl)phenoxy)acetaldehyde O-methyl oxime

Guidance literature:: With lithium hydroxide monohydrate; water; In tetrahydrofuran; methanol; at 0 - 20 ℃; for 1h;

Reference yield: 96.2%

: (2R,3R,4R,5S,6S)-2-(acetoxymethyl)-6-(4-chloro-3-(4-(2-(methoxyimino)ethoxy)benzyl)phenyl)tetrahydro-2H-pyran-3,4,5-triyl triacetate

: 1426924-84-6
2-(4-(2-chloro-5-((2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)benzyl)phenoxy)acetaldehyde O-methyl oxime

Guidance literature:: With lithium hydroxide monohydrate; In tetrahydrofuran; methanol; water; at 0 - 20 ℃; for 1h;

Reference yield:

: 32469-28-6,55515-28-1,55515-29-2,32384-65-9
(3R,4S,5R,6R)-3,4,5-tris((trimethylsilyl)oxy)-6-(((trimethylsilyl)oxy)methyl)tetrahydro-2H-pyran-2-one

: 1426924-84-6
2-(4-(2-chloro-5-((2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)benzyl)phenoxy)acetaldehyde O-methyl oxime

Guidance literature:: Multi-step reaction with 8 steps

1.1: n-butyllithium / tetrahydrofuran; pentane / 0.5 h / -78 °C

1.2: 4 h / -78 °C

1.3: 16 h / 20 °C

2.1: N-ethyl-N,N-diisopropylamine; dmap / tetrahydrofuran / 2 h / 0 - 20 °C

3.1: boron trifluoride diethyl etherate; triethylsilane / water; acetonitrile / 16 h / 10 - 20 °C

4.1: caesium carbonate / N,N-dimethyl-formamide / 36 h / 20 °C

5.1: acetic acid / tetrahydrofuran; water / 24 h / 0 - 20 °C

6.1: oxalyl dichloride / dichloromethane; dimethyl sulfoxide / 1.08 h / -78 °C / Inert atmosphere

7.1: pyridine; sodium acetate / ethanol / 5 h / Inert atmosphere; Reflux

8.1: lithium hydroxide monohydrate / tetrahydrofuran; water; methanol / 1 h / 0 - 20 °C

With pyridine; triethylsilane; dmap; n-butyllithium; oxalyl dichloride; lithium hydroxide monohydrate; boron trifluoride diethyl etherate; sodium acetate; caesium carbonate; acetic acid; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; methanol; ethanol; dichloromethane; water; dimethyl sulfoxide; N,N-dimethyl-formamide; acetonitrile; pentane;