tert-butyl 1-(2-(4-tert-butylcyclohexylidene)ethyl)hydrazinecarboxylate

Base Information

Chemical Name:tert-butyl 1-(2-(4-tert-butylcyclohexylidene)ethyl)hydrazinecarboxylate
CAS No.:1332864-90-0
Molecular Formula:C₁₇H₃₂N₂O₂
Molecular Weight:296.453
Hs Code.:

Synonyms:tert-butyl 1-(2-(4-tert-butylcyclohexylidene)ethyl)hydrazinecarboxylate

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Chemical Property of tert-butyl 1-(2-(4-tert-butylcyclohexylidene)ethyl)hydrazinecarboxylate

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Technology Process of tert-butyl 1-(2-(4-tert-butylcyclohexylidene)ethyl)hydrazinecarboxylate

There total 3 articles about tert-butyl 1-(2-(4-tert-butylcyclohexylidene)ethyl)hydrazinecarboxylate 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:

: 1332864-89-7
C₂₅H₃₀Cl₄N₂O₄

: 1332864-90-0
tert-butyl 1-(2-(4-tert-butylcyclohexylidene)ethyl)hydrazinecarboxylate

Guidance literature:: With ethylenediamine; In tetrahydrofuran; at 0 - 20 ℃; Inert atmosphere;
DOI:10.1021/ja2066219

Reference yield:

: 41498-18-4,85048-19-7,145549-19-5
2-(4-(tert-butyl)cyclohexylidene)ethanol

: 1332864-90-0
tert-butyl 1-(2-(4-tert-butylcyclohexylidene)ethyl)hydrazinecarboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: di-isopropyl azodicarboxylate; triphenylphosphine / tetrahydrofuran / 0 - 20 °C / Inert atmosphere

2: ethylenediamine / tetrahydrofuran / 0 - 20 °C / Inert atmosphere

With di-isopropyl azodicarboxylate; ethylenediamine; triphenylphosphine; In tetrahydrofuran;
DOI:10.1021/ja2066219

Reference yield:

: tert-butyl N-(4,5,6,7-tetrachloro-1,3-dioxoisoindolin-2-yl)carbamate

: 1332864-90-0
tert-butyl 1-(2-(4-tert-butylcyclohexylidene)ethyl)hydrazinecarboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: di-isopropyl azodicarboxylate; triphenylphosphine / tetrahydrofuran / 0 - 20 °C / Inert atmosphere

2: ethylenediamine / tetrahydrofuran / 0 - 20 °C / Inert atmosphere

With di-isopropyl azodicarboxylate; ethylenediamine; triphenylphosphine; In tetrahydrofuran;
DOI:10.1021/ja2066219