1-Methoxy-4-{(1R,2S,3S,4R,5S,6R)-2,3,4,6-tetrakis-benzyloxy-5-[((Z)-propenyl)oxy]-cyclohexyloxymethyl}-benzene

Base Information

Chemical Name:1-Methoxy-4-{(1R,2S,3S,4R,5S,6R)-2,3,4,6-tetrakis-benzyloxy-5-[((Z)-propenyl)oxy]-cyclohexyloxymethyl}-benzene
CAS No.:187841-23-2
Molecular Formula:C₄₅H₄₈O₇
Molecular Weight:700.872
Hs Code.:

Synonyms:1-Methoxy-4-{(1R,2S,3S,4R,5S,6R)-2,3,4,6-tetrakis-benzyloxy-5-[((Z)-propenyl)oxy]-cyclohexyloxymethyl}-benzene

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Chemical Property of 1-Methoxy-4-{(1R,2S,3S,4R,5S,6R)-2,3,4,6-tetrakis-benzyloxy-5-[((Z)-propenyl)oxy]-cyclohexyloxymethyl}-benzene

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Technology Process of 1-Methoxy-4-{(1R,2S,3S,4R,5S,6R)-2,3,4,6-tetrakis-benzyloxy-5-[((Z)-propenyl)oxy]-cyclohexyloxymethyl}-benzene

There total 18 articles about 1-Methoxy-4-{(1R,2S,3S,4R,5S,6R)-2,3,4,6-tetrakis-benzyloxy-5-[((Z)-propenyl)oxy]-cyclohexyloxymethyl}-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:

: 187841-22-1
1D-1-O-allyl-2,4,5,6-tetra-O-benzyl-3-O-p-methoxybenzyl-myo-inositol

: 187841-23-2
1-Methoxy-4-{(1R,2S,3S,4R,5S,6R)-2,3,4,6-tetrakis-benzyloxy-5-[((Z)-propenyl)oxy]-cyclohexyloxymethyl}-benzene

Guidance literature:: With potassium tert-butylate; In dimethyl sulfoxide; at 50 ℃; for 3h;
DOI:10.1016/S0008-6215(96)00211-X

Reference yield:

: 100-39-0
benzyl bromide

: 187841-23-2
1-Methoxy-4-{(1R,2S,3S,4R,5S,6R)-2,3,4,6-tetrakis-benzyloxy-5-[((Z)-propenyl)oxy]-cyclohexyloxymethyl}-benzene

Guidance literature:: Multi-step reaction with 2 steps

1: NaH / dimethylformamide

2: KOBu-t / dimethylsulfoxide / 3 h / 50 °C

With potassium tert-butylate; sodium hydride; In dimethyl sulfoxide; N,N-dimethyl-formamide;
DOI:10.1016/S0008-6215(96)00211-X

Reference yield:

: 140887-04-3
(+/-)-2,5,6-Tri-O-benzyl-3,4-O-isopropylidene-1-O-p-methoxybenzyl-myo-inositol

: 187841-23-2
1-Methoxy-4-{(1R,2S,3S,4R,5S,6R)-2,3,4,6-tetrakis-benzyloxy-5-[((Z)-propenyl)oxy]-cyclohexyloxymethyl}-benzene

Guidance literature:: Multi-step reaction with 4 steps

2: 62 percent / Bu₂SnO, Bu₄NBr / acetonitrile / 10 h / Heating

3: NaH / dimethylformamide

4: KOBu-t / dimethylsulfoxide / 3 h / 50 °C

With potassium tert-butylate; tetrabutylammomium bromide; sodium hydride; di(n-butyl)tin oxide; In dimethyl sulfoxide; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1016/S0008-6215(96)00211-X