1-((1S,2S,3S,4R,5S,6S)-2-Allyloxy-3,4,5,6-tetrakis-benzyloxy-cyclohexyloxymethyl)-4-methoxy-benzene

Base Information

Chemical Name:1-((1S,2S,3S,4R,5S,6S)-2-Allyloxy-3,4,5,6-tetrakis-benzyloxy-cyclohexyloxymethyl)-4-methoxy-benzene
CAS No.:202845-40-7
Molecular Formula:C₄₅H₄₈O₇
Molecular Weight:700.872
Hs Code.:

Synonyms:1-((1S,2S,3S,4R,5S,6S)-2-Allyloxy-3,4,5,6-tetrakis-benzyloxy-cyclohexyloxymethyl)-4-methoxy-benzene

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 1-((1S,2S,3S,4R,5S,6S)-2-Allyloxy-3,4,5,6-tetrakis-benzyloxy-cyclohexyloxymethyl)-4-methoxy-benzene

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Technology Process of 1-((1S,2S,3S,4R,5S,6S)-2-Allyloxy-3,4,5,6-tetrakis-benzyloxy-cyclohexyloxymethyl)-4-methoxy-benzene

There total 9 articles about 1-((1S,2S,3S,4R,5S,6S)-2-Allyloxy-3,4,5,6-tetrakis-benzyloxy-cyclohexyloxymethyl)-4-methoxy-benzene 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: 90.0%

: 851770-80-4
1-O-allyl-3,4,5-tri-O-benzyl-2-O-(4-methoxybenzyl)-D-myo-inositol

: 100-39-0
benzyl bromide

: 202845-40-7
1-((1S,2S,3S,4R,5S,6S)-2-Allyloxy-3,4,5,6-tetrakis-benzyloxy-cyclohexyloxymethyl)-4-methoxy-benzene

Guidance literature:: With sodium hydride; In N,N-dimethyl-formamide; at 0 ℃;
DOI:10.1002/cbic.201500103

Reference yield: 51.0%

: 100-39-0
benzyl bromide

: 202845-42-9
1-O-allyl-3,4,5-tri-O-benzyl-D-myo-inositol

: 132437-55-9
1-O-allyl-2,3,4,5,6-penta-O-benzyl-D-myo-inositol

: 202845-40-7
1-((1S,2S,3S,4R,5S,6S)-2-Allyloxy-3,4,5,6-tetrakis-benzyloxy-cyclohexyloxymethyl)-4-methoxy-benzene

Guidance literature:: With tetra-(n-butyl)ammonium iodide; sodium hydride; In N,N-dimethyl-formamide; 1.) 0 deg C, 2 h, 2.) r.t.;
DOI:10.1039/a800282g

Reference yield: 20.0%

: 100-39-0
benzyl bromide

: 824-94-2
p-methoxybenzyl chloride

: 202845-42-9
1-O-allyl-3,4,5-tri-O-benzyl-D-myo-inositol

: 132437-55-9
1-O-allyl-2,3,4,5,6-penta-O-benzyl-D-myo-inositol

: 202845-40-7
1-((1S,2S,3S,4R,5S,6S)-2-Allyloxy-3,4,5,6-tetrakis-benzyloxy-cyclohexyloxymethyl)-4-methoxy-benzene

Guidance literature:: With tetra-(n-butyl)ammonium iodide; sodium hydride; Yield given. Multistep reaction; 1.) DMF, 0 deg C, 2 h, 2.) r.t.;
DOI:10.1039/a800282g