myo-Inositol, 4-O-(4-methoxyphenyl)methyl-1,3-O-methylene-2,6-bis-O-(phenylmethyl)-5-O-2-propenyl-

Base Information

Chemical Name:myo-Inositol, 4-O-(4-methoxyphenyl)methyl-1,3-O-methylene-2,6-bis-O-(phenylmethyl)-5-O-2-propenyl-
CAS No.:196302-87-1
Molecular Formula:C₃₂H₃₆O₇
Molecular Weight:532.634
Hs Code.:

Synonyms:myo-Inositol, 4-O-(4-methoxyphenyl)methyl-1,3-O-methylene-2,6-bis-O-(phenylmethyl)-5-O-2-propenyl-

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Chemical Property of myo-Inositol, 4-O-(4-methoxyphenyl)methyl-1,3-O-methylene-2,6-bis-O-(phenylmethyl)-5-O-2-propenyl-

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Technology Process of myo-Inositol, 4-O-(4-methoxyphenyl)methyl-1,3-O-methylene-2,6-bis-O-(phenylmethyl)-5-O-2-propenyl-

There total 8 articles about myo-Inositol, 4-O-(4-methoxyphenyl)methyl-1,3-O-methylene-2,6-bis-O-(phenylmethyl)-5-O-2-propenyl- 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: 97.0%

: 106-95-6
allyl bromide

: 196302-84-8
(1R*,5R*,6R*,7S*,8S*,9R*)-8,9-bis(benzyloxy)-6-<(4'-methoxyphenyl)methoxy>-2,4-dioxabicyclo<3.3.1>nonan-7-ol

: 196302-87-1
(1R*,5R*,6S*,7S*,8R*,9R*)-6,9-bis(benzyloxy)-8-<(4'-methoxyphenyl)methoxy>-7-(prop-2'-enyl)-2,4-dioxabicyclo<3.3.1>nonane

Guidance literature:: With sodium hydride; In N,N-dimethyl-formamide; at 0 - 20 ℃;
DOI:10.1039/a703044d

Reference yield:

: myo-inositol-1,3,5-O-orthoformate

: 196302-87-1
(1R*,5R*,6S*,7S*,8R*,9R*)-6,9-bis(benzyloxy)-8-<(4'-methoxyphenyl)methoxy>-7-(prop-2'-enyl)-2,4-dioxabicyclo<3.3.1>nonane

Guidance literature:: Multi-step reaction with 4 steps

1: 69 percent / NaH / dimethylformamide / 1.) 5 deg C, 10 min; r.t., 30 min, 2.) r.t., 4 h

2: 93 percent / NaH / dimethylformamide / 1.) r.t., 1 h, 2.) r.t., 1 h

3: 94 percent / DIBAL-H / hexane; CH₂Cl₂ / 1.) 0 deg C, 15 min, 2.) r.t., 7 h

4: 94 percent / NaH, imidazole / dimethylformamide / 1.) r.t., 30 min, 2.) r.t., 24 h

With 1H-imidazole; sodium hydride; diisobutylaluminium hydride; In hexane; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 125288-07-5,196302-82-6
(1R*,3S*,5R*,6R*,7S*,8R*,9R*)-6-<(4'-methoxyphenyl)methoxy>-2,4,10-trioxatricyclo<3.3.1.1^3,7>decane-8,9-diol

: 196302-87-1
(1R*,5R*,6S*,7S*,8R*,9R*)-6,9-bis(benzyloxy)-8-<(4'-methoxyphenyl)methoxy>-7-(prop-2'-enyl)-2,4-dioxabicyclo<3.3.1>nonane

Guidance literature:: Multi-step reaction with 3 steps

1: 93 percent / NaH / dimethylformamide / 1.) r.t., 1 h, 2.) r.t., 1 h

2: 94 percent / DIBAL-H / hexane; CH₂Cl₂ / 1.) 0 deg C, 15 min, 2.) r.t., 7 h

3: 94 percent / NaH, imidazole / dimethylformamide / 1.) r.t., 30 min, 2.) r.t., 24 h

With 1H-imidazole; sodium hydride; diisobutylaluminium hydride; In hexane; dichloromethane; N,N-dimethyl-formamide;