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1-benzyl-3-tert-butoxycarbonylaminooxindole

Base Information Edit
  • Chemical Name:1-benzyl-3-tert-butoxycarbonylaminooxindole
  • CAS No.:1620145-28-9
  • Molecular Formula:C20H22N2O3
  • Molecular Weight:338.406
  • Hs Code.:
  • Mol file:1620145-28-9.mol
1-benzyl-3-tert-butoxycarbonylaminooxindole

Synonyms:1-benzyl-3-tert-butoxycarbonylaminooxindole

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Chemical Property of 1-benzyl-3-tert-butoxycarbonylaminooxindole Edit
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Technology Process of 1-benzyl-3-tert-butoxycarbonylaminooxindole

There total 1 articles about 1-benzyl-3-tert-butoxycarbonylaminooxindole 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:
Guidance literature:
1-benzyl-3-(hydroxyimino)indolin-2-one; With palladium 10% on activated carbon; hydrogen; In methanol; at 20 ℃; for 10h;
di-tert-butyl dicarbonate; In methanol; at 20 ℃; Inert atmosphere;
DOI:10.1016/j.tet.2021.132163
Guidance literature:
methyl 2-{[(tert-butoxycarbonyl)oxy](phenyl)methyl}acrylate; 1-benzyl-3-tert-butoxycarbonylaminooxindole; With 4-(3-ethyl-4-oxa-1-azatricyclo[4,4,0,0(3,8)]dec-5-yl)quinolin-6-ol; In Hexafluorobenzene; at 20 ℃; for 12h;
With water; toluene-4-sulfonic acid; In Hexafluorobenzene; at 50 ℃; for 5h; Solvent; Reagent/catalyst; enantioselective reaction;
DOI:10.1016/j.tet.2021.132163
Guidance literature:
C20H22O5; 1-benzyl-3-tert-butoxycarbonylaminooxindole; With 4-(3-ethyl-4-oxa-1-azatricyclo[4,4,0,0(3,8)]dec-5-yl)quinolin-6-ol; In Hexafluorobenzene; at 20 ℃; for 24h;
With water; toluene-4-sulfonic acid; In Hexafluorobenzene; at 50 ℃; for 7h; enantioselective reaction;
DOI:10.1016/j.tet.2021.132163
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