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N-tert-butyloxycarbonylaminoisophthalimide

Base Information
  • Chemical Name:N-tert-butyloxycarbonylaminoisophthalimide
  • CAS No.:109473-36-1
  • Molecular Formula:C13H14N2O4
  • Molecular Weight:262.265
  • Hs Code.:
N-tert-butyloxycarbonylaminoisophthalimide

Synonyms:N-tert-butyloxycarbonylaminoisophthalimide

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Chemical Property of N-tert-butyloxycarbonylaminoisophthalimide
Chemical Property:
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MSDS Files:

SDS file from LookChem

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Technology Process of N-tert-butyloxycarbonylaminoisophthalimide

There total 1 articles about N-tert-butyloxycarbonylaminoisophthalimide 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:
Multi-step reaction with 2 steps
1: 100 percent / tetrahydrofuran / 0.08 h / 20 °C
2: 82 percent / 1,3-dicyclohexylcarbodiimide / tetrahydrofuran / 1 h
With dicyclohexyl-carbodiimide; In tetrahydrofuran; 1: Acylation / 2: Cyclization;
DOI:10.1021/jo000225s
Guidance literature:
Multi-step reaction with 3 steps
1: acetic acid; triethylamine / tetrahydrofuran / 1 h / Heating
2: 97 percent / triphenylphosphine; diethyl azodicarboxylate / tetrahydrofuran / 0.5 h / 0 - 5 °C
3: 65 percent / methylhydrazine / tetrahydrofuran / 0 - 20 °C
With acetic acid; triethylamine; triphenylphosphine; methylhydrazine; diethylazodicarboxylate; In tetrahydrofuran; 1: Isomerization / 2: Methylation / 3: dephthaloylation;
DOI:10.1021/jo000225s
Guidance literature:
Multi-step reaction with 3 steps
1: acetic acid; triethylamine / tetrahydrofuran / 1 h / Heating
2: 83 percent / triphenylphosphine; diethyl azodicarboxylate / tetrahydrofuran / 0.5 h / 0 - 5 °C
3: 65 percent / methylhydrazine / tetrahydrofuran / 0 - 20 °C
With acetic acid; triethylamine; triphenylphosphine; methylhydrazine; diethylazodicarboxylate; In tetrahydrofuran; 1: Isomerization / 2: Alkylation / 3: dephthaloylation;
DOI:10.1021/jo000225s
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