(2S,3S,4S,5R,6S)-6-(3-(4-(allyloxy)benzyl)-4-chlorophenyl)-3,4,5-trihydroxy-6-methoxytetrahydro-2H-pyran-2-carbaldehyde

Base Information

Chemical Name:(2S,3S,4S,5R,6S)-6-(3-(4-(allyloxy)benzyl)-4-chlorophenyl)-3,4,5-trihydroxy-6-methoxytetrahydro-2H-pyran-2-carbaldehyde
CAS No.:1416165-19-9
Molecular Formula:C₂₃H₂₅ClO₇
Molecular Weight:448.9
Hs Code.:

Synonyms:(2S,3S,4S,5R,6S)-6-(3-(4-(allyloxy)benzyl)-4-chlorophenyl)-3,4,5-trihydroxy-6-methoxytetrahydro-2H-pyran-2-carbaldehyde

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Chemical Property of (2S,3S,4S,5R,6S)-6-(3-(4-(allyloxy)benzyl)-4-chlorophenyl)-3,4,5-trihydroxy-6-methoxytetrahydro-2H-pyran-2-carbaldehyde

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Technology Process of (2S,3S,4S,5R,6S)-6-(3-(4-(allyloxy)benzyl)-4-chlorophenyl)-3,4,5-trihydroxy-6-methoxytetrahydro-2H-pyran-2-carbaldehyde

There total 4 articles about (2S,3S,4S,5R,6S)-6-(3-(4-(allyloxy)benzyl)-4-chlorophenyl)-3,4,5-trihydroxy-6-methoxytetrahydro-2H-pyran-2-carbaldehyde 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:

: 1426924-93-7
((2R,3S,4S,5R,6S)-6-(3-(4-(allyloxy)benzyl)-4-chlorophenyl)-3,4,5-trihydroxy-6-methoxytetrahydro-2H-pyran-2-yl)methyl 4-methylbenzenesulfonate

: 1416165-19-9
(2S,3S,4S,5R,6S)-6-(3-(4-(allyloxy)benzyl)-4-chlorophenyl)-3,4,5-trihydroxy-6-methoxytetrahydro-2H-pyran-2-carbaldehyde

Guidance literature:: With collidine; In dimethyl sulfoxide; at 150 ℃; for 0.75h;

Reference yield:

: 864070-18-8
4-(5-bromo-2-chlorobenzyl)phenol

: 1416165-19-9
(2S,3S,4S,5R,6S)-6-(3-(4-(allyloxy)benzyl)-4-chlorophenyl)-3,4,5-trihydroxy-6-methoxytetrahydro-2H-pyran-2-carbaldehyde

Guidance literature:: Multi-step reaction with 4 steps

1.1: caesium carbonate / N,N-dimethyl-formamide / 2 h / 0 - 20 °C

2.1: n-butyllithium / tetrahydrofuran; hexanes / 0.5 h / -78 °C / Inert atmosphere

2.2: 3 h / -78 °C

2.3: 16 h / 20 °C

3.1: leutidine / 12 h / 0 - 20 °C

4.1: collidine / dimethyl sulfoxide / 0.75 h / 150 °C

With n-butyllithium; caesium carbonate; In tetrahydrofuran; hexanes; dimethyl sulfoxide; N,N-dimethyl-formamide;

Reference yield:

: 1416165-17-7
(2S,3R,4S,5S,6R)-2-(3-(4-(allyloxy)benzyl)-4-chlorophenyl)-6-(hydroxy methyl)-2-methoxytetrahydro-2H-pyran-3,4,5-triol

: 1416165-19-9
(2S,3S,4S,5R,6S)-6-(3-(4-(allyloxy)benzyl)-4-chlorophenyl)-3,4,5-trihydroxy-6-methoxytetrahydro-2H-pyran-2-carbaldehyde

Guidance literature:: Multi-step reaction with 2 steps

1: leutidine / 12 h / 0 - 20 °C

2: collidine / dimethyl sulfoxide / 0.75 h / 150 °C

With leutidine; collidine; In dimethyl sulfoxide;