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

Base Information

• Chemical Name: (3aR,4R,6S,7aS)-4-Allyl-6-benzyloxymethyl-2,2-dimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran
• CAS No.: 147806-42-6
• Molecular Formula: C₁₉H₂₆O₄
• Molecular Weight: 318.413
• Mol file: 147806-42-6.mol

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

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

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

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

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

benzyl bromide (100-39-0) + ((3aR,4R,6S,7aS)-4-Allyl-2,2-dimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran-6-yl)-methanol (132375-56-5) → (3aR,4R,6S,7aS)-4-Allyl-6-benzyloxymethyl-2,2-dimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran (147806-42-6)

Guidance literature:

With tetra-(n-butyl)ammonium iodide; sodium hydride; In tetrahydrofuran; at 25 ℃; for 24h;

DOI:10.1021/ja00046a063

Reference yield:

2,6-Anhydro-1-O-(tert-butyldiphenylsilyl)-3,7,8,9-tetradeoxy-4,5-O-isopropylidene-D-altro-non-8-enitol (122821-81-2) → (3aR,4R,6S,7aS)-4-Allyl-6-benzyloxymethyl-2,2-dimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran (147806-42-6)

Guidance literature:

Multi-step reaction with 2 steps

1: 80 percent / TBAF / tetrahydrofuran / 1 h / 25 °C

2: 90 percent / NaH, n-Bu₄NI / tetrahydrofuran / 24 h / 25 °C

With tetrabutyl ammonium fluoride; tetra-(n-butyl)ammonium iodide; sodium hydride; In tetrahydrofuran;

Reference yield: 98.0%

(3aR,4R,6S,7aS)-4-Allyl-6-benzyloxymethyl-2,2-dimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyran (147806-42-6) → (2R,3S,4S,6S)-2-Allyl-6-benzyloxymethyl-tetrahydro-pyran-3,4-diol (147806-43-7)

Guidance literature:

With trifluoroacetic acid; In toluene; at 0 ℃; for 0.25h;

upstream raw materials:

benzyl bromide

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

2,6-Anhydro-1-O-(tert-butyldiphenylsilyl)-3,7,8,9-tetradeoxy-4,5-O-isopropylidene-D-altro-non-8-enitol

Downstream raw materials:

(2R,3S,4S,6S)-2-Allyl-6-benzyloxymethyl-tetrahydro-pyran-3,4-diol

Hemibrevetoxin-B

(2R,3S,4S,6S)-2-allyl-4-benzyloxy-6-benzyloxymethyl-tetrahydropyran-3-ol

3,4:6,10-dianhydro-8,11-O-dibenzyl-3-C-methyl-1,2,5,9-tetradeoxy-D-threo-L-altro-undec-1-enitol