di-tert-butyl 2,2’-(1,4-phenylenebis(methanylylidene)) bis (N-isopropylhydrazinecarboxamide)

Base Information

Chemical Name:di-tert-butyl 2,2’-(1,4-phenylenebis(methanylylidene)) bis (N-isopropylhydrazinecarboxamide)
CAS No.:1448899-63-5
Molecular Formula:C₁₆H₂₄N₆O₂
Molecular Weight:332.406
Hs Code.:

Synonyms:di-tert-butyl 2,2’-(1,4-phenylenebis(methanylylidene)) bis (N-isopropylhydrazinecarboxamide)

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of di-tert-butyl 2,2’-(1,4-phenylenebis(methanylylidene)) bis (N-isopropylhydrazinecarboxamide)

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Technology Process of di-tert-butyl 2,2’-(1,4-phenylenebis(methanylylidene)) bis (N-isopropylhydrazinecarboxamide)

There total 2 articles about di-tert-butyl 2,2’-(1,4-phenylenebis(methanylylidene)) bis (N-isopropylhydrazinecarboxamide) 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: 82.0%

: 1448899-71-5
di-tert-butyl 2,2’-(1,4-phenylenebis(methanylylidene))bis(hydrazinecarboxylate)

: 75-31-0
isopropylamine

: 1448899-63-5
di-tert-butyl 2,2’-(1,4-phenylenebis(methanylylidene)) bis (N-isopropylhydrazinecarboxamide)

Guidance literature:: In acetonitrile; at 150 ℃; for 6h; Inert atmosphere; Microwave irradiation;
DOI:10.1021/ol4016089

Reference yield:

: 623-27-8
terephthalaldehyde,

: 1448899-63-5
di-tert-butyl 2,2’-(1,4-phenylenebis(methanylylidene)) bis (N-isopropylhydrazinecarboxamide)

Guidance literature:: Multi-step reaction with 2 steps

1: acetic acid / methanol / Reflux

2: acetonitrile / 6 h / 150 °C / Inert atmosphere; Microwave irradiation

With acetic acid; In methanol; acetonitrile;
DOI:10.1021/ol4016089