C₈₀H₉₆O₁₂

Base Information

Chemical Name:C₈₀H₉₆O₁₂
CAS No.:160848-32-8
Molecular Formula:C₈₀H₉₆O₁₂
Molecular Weight:1249.64
Hs Code.:

C<sub>80</sub>H<sub>96</sub>O<sub>12</sub>

Synonyms:C₈₀H₉₆O₁₂

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Chemical Property of C₈₀H₉₆O₁₂

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Technology Process of C₈₀H₉₆O₁₂

There total 12 articles about C₈₀H₉₆O₁₂ 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: 59.0%

: 86795-39-3
(2S,3R,4R,5S,6S)-3,4,5-tris(benzyloxy)-2-chloro-6-methyltetrahydro-2H-pyran

: 160848-31-7
C₅₃H₆₈O₈

: 160848-32-8
C₈₀H₉₆O₁₂

Guidance literature:: With isopropenylbenzene; at 80 ℃; for 60h;
DOI:10.1021/jo00107a018

Reference yield:

: 40246-26-2
3,4,6-tri-O-benzyl-α-D-glucopyranose

: 160848-32-8
C₈₀H₉₆O₁₂

Guidance literature:: Multi-step reaction with 3 steps

1: SOCl₂ / dimethylformamide; CH₂Cl₂ / 3 h / 0 °C

2: 59 percent / tetramethylurea, TfOH / CH₂Cl₂ / 168 h / 25 °C

3: 59 percent / α-methylstyrene / 60 h / 80 °C

With thionyl chloride; trifluorormethanesulfonic acid; tetramethylurea; isopropenylbenzene; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jo00107a018

Reference yield:

: 228702-12-3
1,2-O-ethylidene(R,S)-α-D-glucopyranose

: 160848-32-8
C₈₀H₉₆O₁₂

Guidance literature:: Multi-step reaction with 5 steps

1: KOH / dioxane / 0.08 h / Heating

2: 80percent AcOH / 36 h / 90 °C

3: SOCl₂ / dimethylformamide; CH₂Cl₂ / 3 h / 0 °C

4: 59 percent / tetramethylurea, TfOH / CH₂Cl₂ / 168 h / 25 °C

5: 59 percent / α-methylstyrene / 60 h / 80 °C

With potassium hydroxide; thionyl chloride; trifluorormethanesulfonic acid; acetic acid; tetramethylurea; isopropenylbenzene; In 1,4-dioxane; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jo00107a018