(1R,2R,3R)-1-(3,4-Dimethoxy-phenyl)-6,7-dimethoxy-1,2,3,4-tetrahydro-naphthalene-2,3-dicarboxylic acid bis-((S)-methoxycarbonyl-phenyl-methyl) ester

Base Information

Chemical Name:(1R,2R,3R)-1-(3,4-Dimethoxy-phenyl)-6,7-dimethoxy-1,2,3,4-tetrahydro-naphthalene-2,3-dicarboxylic acid bis-((S)-methoxycarbonyl-phenyl-methyl) ester
CAS No.:175293-58-0
Molecular Formula:C₄₀H₄₀O₁₂
Molecular Weight:712.75
Hs Code.:

(1R,2R,3R)-1-(3,4-Dimethoxy-phenyl)-6,7-dimethoxy-1,2,3,4-tetrahydro-naphthalene-2,3-dicarboxylic acid bis-((S)-methoxycarbonyl-phenyl-methyl) ester

Synonyms:

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Chemical Property of (1R,2R,3R)-1-(3,4-Dimethoxy-phenyl)-6,7-dimethoxy-1,2,3,4-tetrahydro-naphthalene-2,3-dicarboxylic acid bis-((S)-methoxycarbonyl-phenyl-methyl) ester

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Technology Process of (1R,2R,3R)-1-(3,4-Dimethoxy-phenyl)-6,7-dimethoxy-1,2,3,4-tetrahydro-naphthalene-2,3-dicarboxylic acid bis-((S)-methoxycarbonyl-phenyl-methyl) ester

There total 1 articles about (1R,2R,3R)-1-(3,4-Dimethoxy-phenyl)-6,7-dimethoxy-1,2,3,4-tetrahydro-naphthalene-2,3-dicarboxylic acid bis-((S)-methoxycarbonyl-phenyl-methyl) 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:

: 175293-57-9
(1R,2S,3R)-1-(3,4-Dimethoxy-phenyl)-1-hydroxy-6,7-dimethoxy-1,2,3,4-tetrahydro-naphthalene-2,3-dicarboxylic acid bis-((S)-methoxycarbonyl-phenyl-methyl) ester

: 175293-58-0
(1R,2R,3R)-1-(3,4-Dimethoxy-phenyl)-6,7-dimethoxy-1,2,3,4-tetrahydro-naphthalene-2,3-dicarboxylic acid bis-((S)-methoxycarbonyl-phenyl-methyl) ester

Guidance literature:: With lithium aluminium tetrahydride; boron trifluoride diethyl etherate; Yield given. Multistep reaction; 1.) dichloromethane, -20 deg C, 2.) dichloromethane, ether, -55 deg C, 20 min;
DOI:10.1139/v96-011

Reference yield:

: 175293-58-0
(1R,2R,3R)-1-(3,4-Dimethoxy-phenyl)-6,7-dimethoxy-1,2,3,4-tetrahydro-naphthalene-2,3-dicarboxylic acid bis-((S)-methoxycarbonyl-phenyl-methyl) ester

: 59573-53-4
isolariciresinol dimethyl ether

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) NaOMe, 2.) HCl / 1.) reflux, 23 h, 2.) 12 h

2: 96 percent / LiAlH₄ / tetrahydrofuran / 2 h / Heating

With hydrogenchloride; lithium aluminium tetrahydride; sodium methylate; In tetrahydrofuran;
DOI:10.1139/v96-011

Reference yield:

: 67-56-1
methanol

: 175293-58-0
(1R,2R,3R)-1-(3,4-Dimethoxy-phenyl)-6,7-dimethoxy-1,2,3,4-tetrahydro-naphthalene-2,3-dicarboxylic acid bis-((S)-methoxycarbonyl-phenyl-methyl) ester

: 59527-51-4
(1R,2S,3S)-1-(3,4-Dimethoxy-phenyl)-6,7-dimethoxy-1,2,3,4-tetrahydro-naphthalene-2,3-dicarboxylic acid dimethyl ester

Guidance literature:: With hydrogenchloride; sodium methylate; Yield given. Multistep reaction; 1.) reflux, 23 h, 2.) 12 h;
DOI:10.1139/v96-011