((3aS,4R,6R,7S,7aR)-6-Allyl-7-benzyloxy-2,2-dimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-4-yl)-methanol

Base Information

Chemical Name:((3aS,4R,6R,7S,7aR)-6-Allyl-7-benzyloxy-2,2-dimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-4-yl)-methanol
CAS No.:475276-03-0
Molecular Formula:C₁₉H₂₆O₅
Molecular Weight:334.412
Hs Code.:

Synonyms:((3aS,4R,6R,7S,7aR)-6-Allyl-7-benzyloxy-2,2-dimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-4-yl)-methanol

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Chemical Property of ((3aS,4R,6R,7S,7aR)-6-Allyl-7-benzyloxy-2,2-dimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-4-yl)-methanol

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Technology Process of ((3aS,4R,6R,7S,7aR)-6-Allyl-7-benzyloxy-2,2-dimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-4-yl)-methanol

There total 6 articles about ((3aS,4R,6R,7S,7aR)-6-Allyl-7-benzyloxy-2,2-dimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-4-yl)-methanol 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: 100.0%

: 475276-02-9
((3aS,4R,6R,7S,7aR)-6-Allyl-7-benzyloxy-2,2-dimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-4-ylmethoxy)-tert-butyl-diphenyl-silane

: 475276-03-0
((3aS,4R,6R,7S,7aR)-6-Allyl-7-benzyloxy-2,2-dimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-4-yl)-methanol

Guidance literature:: With tetrabutyl ammonium fluoride; In tetrahydrofuran; at 23 ℃; for 2h;
DOI:10.1055/s-2002-33511

Reference yield:

: 53263-18-6,82659-53-8,98920-46-8,98920-48-0,98920-49-1,103773-87-1,98920-44-6
allyl 2,3,4,6-tetra-O-acetyl-α-D-galactopyranoside

: 475276-03-0
((3aS,4R,6R,7S,7aR)-6-Allyl-7-benzyloxy-2,2-dimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-4-yl)-methanol

Guidance literature:: Multi-step reaction with 5 steps

1: 89 percent / MeONa / methanol / 48 h / 0 °C

2: imidazole / dimethylformamide / 0.5 h / 24 °C

3: CSA / 1.5 h / 24 °C

4: 99 percent / NaI; Bu₄NI / tetrahydrofuran / 30 h / 24 °C

5: 100 percent / TBAF / tetrahydrofuran / 2 h / 23 °C

With 1H-imidazole; camphor-10-sulfonic acid; tetrabutyl ammonium fluoride; sodium methylate; tetra-(n-butyl)ammonium iodide; sodium iodide; In tetrahydrofuran; methanol; N,N-dimethyl-formamide;
DOI:10.1055/s-2002-33511

Reference yield:

: 133697-14-0
2,6-anhydro-7,8,9-trideoxy-D-glycero-L-galacto-non-8-enitol

: 475276-03-0
((3aS,4R,6R,7S,7aR)-6-Allyl-7-benzyloxy-2,2-dimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-4-yl)-methanol

Guidance literature:: Multi-step reaction with 4 steps

1: imidazole / dimethylformamide / 0.5 h / 24 °C

2: CSA / 1.5 h / 24 °C

3: 99 percent / NaI; Bu₄NI / tetrahydrofuran / 30 h / 24 °C

4: 100 percent / TBAF / tetrahydrofuran / 2 h / 23 °C

With 1H-imidazole; camphor-10-sulfonic acid; tetrabutyl ammonium fluoride; tetra-(n-butyl)ammonium iodide; sodium iodide; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1055/s-2002-33511