D-1-O-acetyl-2,6-di-O-benzyloxymethyl-3,4,5-tri-O-methoxybenzyl-myo-inositol

Base Information

Chemical Name:D-1-O-acetyl-2,6-di-O-benzyloxymethyl-3,4,5-tri-O-methoxybenzyl-myo-inositol
CAS No.:137897-36-0
Molecular Formula:C₄₈H₅₄O₁₂
Molecular Weight:822.95
Hs Code.:

Synonyms:D-1-O-acetyl-2,6-di-O-benzyloxymethyl-3,4,5-tri-O-methoxybenzyl-myo-inositol

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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 D-1-O-acetyl-2,6-di-O-benzyloxymethyl-3,4,5-tri-O-methoxybenzyl-myo-inositol

Chemical Property:

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Technology Process of D-1-O-acetyl-2,6-di-O-benzyloxymethyl-3,4,5-tri-O-methoxybenzyl-myo-inositol

There total 8 articles about D-1-O-acetyl-2,6-di-O-benzyloxymethyl-3,4,5-tri-O-methoxybenzyl-myo-inositol 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: 86.0%

: 3587-60-8
Benzyloxymethyl chloride

: 137897-31-5
D-1-O-acetyl-3,4,5-O-trimethoxybenzyl-myo-inositol

: 137897-36-0
D-1-O-acetyl-2,6-di-O-benzyloxymethyl-3,4,5-tri-O-methoxybenzyl-myo-inositol

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In 1,2-dichloro-ethane; for 3h; Heating;
DOI:10.1021/jo001575h

Reference yield:

: 137897-35-9
(2S,3S,4S,5R,6S)-6-Methoxy-3,4,5-tris-(4-methoxy-benzyloxy)-tetrahydro-pyran-2-carbaldehyde

: 137897-36-0
D-1-O-acetyl-2,6-di-O-benzyloxymethyl-3,4,5-tri-O-methoxybenzyl-myo-inositol

Guidance literature:: Multi-step reaction with 4 steps

1: 5.40 g / Et₃N; 4-(dimethylamino)pyridine / 1,2-dichloro-ethane / 3 h / Heating

2: 28.7 percent / PdCl₂ / H₂O; dioxane / 3 h / 60 °C

3: 96.3 percent / Me₄NBH(OAc)3 / acetonitrile; acetic acid / 3 h / 20 °C

4: 86 percent / N,N-diisopropylethylamine / 1,2-dichloro-ethane / 3 h / Heating

With dmap; triethylamine; N-ethyl-N,N-diisopropylamine; tetramethylammonium triacetoxyborohydride; palladium dichloride; In 1,4-dioxane; water; acetic acid; 1,2-dichloro-ethane; acetonitrile; 2: Ferrier-II rearrangement;
DOI:10.1021/jo001575h

Reference yield:

: 137897-29-1
(Z)-methyl 6-O-acetyl-2,3,4-tri-O-methoxybenzyl-α-D-gluco-hex-5-enopyranoside

: 137897-36-0
D-1-O-acetyl-2,6-di-O-benzyloxymethyl-3,4,5-tri-O-methoxybenzyl-myo-inositol

Guidance literature:: Multi-step reaction with 3 steps

1: 28.7 percent / PdCl₂ / H₂O; dioxane / 3 h / 60 °C

2: 96.3 percent / Me₄NBH(OAc)3 / acetonitrile; acetic acid / 3 h / 20 °C

3: 86 percent / N,N-diisopropylethylamine / 1,2-dichloro-ethane / 3 h / Heating

With N-ethyl-N,N-diisopropylamine; tetramethylammonium triacetoxyborohydride; palladium dichloride; In 1,4-dioxane; water; acetic acid; 1,2-dichloro-ethane; acetonitrile; 1: Ferrier-II rearrangement;
DOI:10.1021/jo001575h