5,6-bis-p-(benzyloxy)benzoyloxy-4,7-di(p-(tert-butyldimethylsilyloxy)phenyl)benzo[d][1,3]dioxol-2-yl acetate

Base Information

Chemical Name:5,6-bis-p-(benzyloxy)benzoyloxy-4,7-di(p-(tert-butyldimethylsilyloxy)phenyl)benzo[d][1,3]dioxol-2-yl acetate
CAS No.:1160726-24-8
Molecular Formula:C₆₁H₆₄O₁₂Si₂
Molecular Weight:1045.34
Hs Code.:

Synonyms:5,6-bis-p-(benzyloxy)benzoyloxy-4,7-di(p-(tert-butyldimethylsilyloxy)phenyl)benzo[d][1,3]dioxol-2-yl acetate

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Chemical Property of 5,6-bis-p-(benzyloxy)benzoyloxy-4,7-di(p-(tert-butyldimethylsilyloxy)phenyl)benzo[d][1,3]dioxol-2-yl acetate

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Technology Process of 5,6-bis-p-(benzyloxy)benzoyloxy-4,7-di(p-(tert-butyldimethylsilyloxy)phenyl)benzo[d][1,3]dioxol-2-yl acetate

There total 1 articles about 5,6-bis-p-(benzyloxy)benzoyloxy-4,7-di(p-(tert-butyldimethylsilyloxy)phenyl)benzo[d][1,3]dioxol-2-yl acetate 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: 85.0%

: 1160726-23-7
5,6-bis-p-(benzyloxy)benzoyloxy-4,7-di(p-(tert-butyldimethylsilyloxy)phenyl)benzo[d][1,3]dioxole

: 546-67-8
lead(IV) tetraacetate

: 1160726-24-8
5,6-bis-p-(benzyloxy)benzoyloxy-4,7-di(p-(tert-butyldimethylsilyloxy)phenyl)benzo[d][1,3]dioxol-2-yl acetate

Guidance literature:: In benzene; at 80 ℃; for 20h; Inert atmosphere;
DOI:10.1021/jo900638b

Reference yield: 76.0%

: 1160726-24-8
5,6-bis-p-(benzyloxy)benzoyloxy-4,7-di(p-(tert-butyldimethylsilyloxy)phenyl)benzo[d][1,3]dioxol-2-yl acetate

: 610769-63-6
thelephantin G

Guidance literature:: 5,6-bis-p-(benzyloxy)benzoyloxy-4,7-di(p-(tert-butyldimethylsilyloxy)phenyl)benzo[d][1,3]dioxol-2-yl acetate; With hydrogenchloride; methanol; In dichloromethane; at 20 ℃; for 14h; Inert atmosphere;

With palladium dihydroxide; hydrogen; In ethyl acetate; at 20 ℃; for 15h;
DOI:10.1021/jo900638b