2-O-benzyl-1-O-benzyloxymethyl-4,6-di-O-p-methoxybenzyl-D-myo-inositol 3,5-bis(dibenzyl phosphate)

Base Information

Chemical Name:2-O-benzyl-1-O-benzyloxymethyl-4,6-di-O-p-methoxybenzyl-D-myo-inositol 3,5-bis(dibenzyl phosphate)
CAS No.:910864-36-7
Molecular Formula:C₆₅H₆₈O₁₅P₂
Molecular Weight:1151.19
Hs Code.:

Synonyms:2-O-benzyl-1-O-benzyloxymethyl-4,6-di-O-p-methoxybenzyl-D-myo-inositol 3,5-bis(dibenzyl phosphate)

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Chemical Property of 2-O-benzyl-1-O-benzyloxymethyl-4,6-di-O-p-methoxybenzyl-D-myo-inositol 3,5-bis(dibenzyl phosphate)

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Technology Process of 2-O-benzyl-1-O-benzyloxymethyl-4,6-di-O-p-methoxybenzyl-D-myo-inositol 3,5-bis(dibenzyl phosphate)

There total 8 articles about 2-O-benzyl-1-O-benzyloxymethyl-4,6-di-O-p-methoxybenzyl-D-myo-inositol 3,5-bis(dibenzyl phosphate) 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: 38.0%

: 910864-35-6
2-O-benzyl-1-O-benzyloxymethyl-4,6-di-O-p-methoxybenzyl-D-myo-inositol 3-diphenyl phosphate 5-dibenzyl phosphate

: 100-51-6,185532-71-2
benzyl alcohol

: 910864-36-7
2-O-benzyl-1-O-benzyloxymethyl-4,6-di-O-p-methoxybenzyl-D-myo-inositol 3,5-bis(dibenzyl phosphate)

Guidance literature:: With sodium hydride; In tetrahydrofuran; at 20 ℃; for 0.5h;
DOI:10.1021/jo0610816

Reference yield:

: 2-O-benzyl-4,6-di-O-p-methoxybenzyl-D-myo-inositol-1,3,5-O-orthoformate

: 910864-36-7
2-O-benzyl-1-O-benzyloxymethyl-4,6-di-O-p-methoxybenzyl-D-myo-inositol 3,5-bis(dibenzyl phosphate)

Guidance literature:: Multi-step reaction with 5 steps

1.1: 55 percent / aq. HCl / methanol / 18 h / 20 °C

2.1: 53 percent / Et₃N / BocHis(Me)-[4S-tBuOPro]-[(CH₂)4-1,4-diylGly]-Tyr(tBu)-PheOMe / toluene

3.1: 36 percent / iPr₂NEt / tetrahydrofuran / 24 h / 50 °C

4.1: 4,5-dicyanoimidazole / CH₂Cl₂ / 15 h / 20 °C

4.2: 81 percent / aq. H₂O₂ / CH₂Cl₂ / 1 h / 0 °C

5.1: 38 percent / NaH / tetrahydrofuran / 0.5 h / 20 °C

With hydrogenchloride; 4,5-dicyano-1H-imidazole; sodium hydride; triethylamine; N-ethyl-N,N-diisopropylamine; BocHis(Me)-[4S-tBuOPro]-[(CH₂)4-1,4-diylGly]-Tyr(tBu)-PheOMe; In tetrahydrofuran; methanol; dichloromethane; toluene;
DOI:10.1021/jo0610816

Reference yield:

: 910864-22-1
2-O-benzyl-4,6-di-O-p-methoxybenzyl-D-myo-inositol

: 910864-36-7
2-O-benzyl-1-O-benzyloxymethyl-4,6-di-O-p-methoxybenzyl-D-myo-inositol 3,5-bis(dibenzyl phosphate)

Guidance literature:: Multi-step reaction with 4 steps

1.1: 53 percent / Et₃N / BocHis(Me)-[4S-tBuOPro]-[(CH₂)4-1,4-diylGly]-Tyr(tBu)-PheOMe / toluene

2.1: 36 percent / iPr₂NEt / tetrahydrofuran / 24 h / 50 °C

3.1: 4,5-dicyanoimidazole / CH₂Cl₂ / 15 h / 20 °C

3.2: 81 percent / aq. H₂O₂ / CH₂Cl₂ / 1 h / 0 °C

4.1: 38 percent / NaH / tetrahydrofuran / 0.5 h / 20 °C

With 4,5-dicyano-1H-imidazole; sodium hydride; triethylamine; N-ethyl-N,N-diisopropylamine; BocHis(Me)-[4S-tBuOPro]-[(CH₂)4-1,4-diylGly]-Tyr(tBu)-PheOMe; In tetrahydrofuran; dichloromethane; toluene;
DOI:10.1021/jo0610816