2-[3,5-bis-(3,5-di-tert-butyl-benzyloxy)-benzyl]-5-nitro-isoindole-1,3-dione

Base Information

Chemical Name:2-[3,5-bis-(3,5-di-tert-butyl-benzyloxy)-benzyl]-5-nitro-isoindole-1,3-dione
CAS No.:301646-75-3
Molecular Formula:C₄₅H₅₄N₂O₆
Molecular Weight:718.934
Hs Code.:

2-[3,5-bis-(3,5-di-<i>tert</i>-butyl-benzyloxy)-benzyl]-5-nitro-isoindole-1,3-dione

Synonyms:2-[3,5-bis-(3,5-di-tert-butyl-benzyloxy)-benzyl]-5-nitro-isoindole-1,3-dione

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Chemical Property of 2-[3,5-bis-(3,5-di-tert-butyl-benzyloxy)-benzyl]-5-nitro-isoindole-1,3-dione

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Technology Process of 2-[3,5-bis-(3,5-di-tert-butyl-benzyloxy)-benzyl]-5-nitro-isoindole-1,3-dione

There total 1 articles about 2-[3,5-bis-(3,5-di-tert-butyl-benzyloxy)-benzyl]-5-nitro-isoindole-1,3-dione 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: 63.0%

: 89-40-7
4-nitrophthalimide

: 213680-85-4
1,3-bis{[3,5-bis(tert-butyl)benzyl]oxy}-5-(bromomethyl)benzene

: 301646-75-3
2-[3,5-bis-(3,5-di-tert-butyl-benzyloxy)-benzyl]-5-nitro-isoindole-1,3-dione

Guidance literature:: With potassium carbonate; In acetonitrile;
DOI:10.1021/ol006157d

Reference yield: 75.0%

: 301646-75-3
2-[3,5-bis-(3,5-di-tert-butyl-benzyloxy)-benzyl]-5-nitro-isoindole-1,3-dione

: 5-amino-2-[3,5-bis-(3,5-di-tert-butyl-benzyloxy)-benzyl]-isoindole-1,3-dione

Guidance literature:: With hydrogen; nickel; In ethanol;
DOI:10.1021/ol006157d

Reference yield:

: 301646-75-3
2-[3,5-bis-(3,5-di-tert-butyl-benzyloxy)-benzyl]-5-nitro-isoindole-1,3-dione

: 301646-76-4
1-{2-[3,5-bis-(3,5-di-tert-butyl-benzyloxy)-benzyl]-1,3-dioxo-2,3-dihydro-1H-isoindol-5-yl}-3-hexyl-urea

Guidance literature:: Multi-step reaction with 2 steps

1: 75 percent / H₂ / Raney Ni / ethanol

2: 50 percent / Et₃N / CH₂Cl₂

With hydrogen; triethylamine; nickel; In ethanol; dichloromethane; 1: Catalytic hydrogenation / 2: Condensation;
DOI:10.1021/ol006157d