<5--3-tert-butyl-2-hydroxyphenylimino>triphenylphosphoran

Base Information

Chemical Name:<5--3-tert-butyl-2-hydroxyphenylimino>triphenylphosphoran
CAS No.:76826-04-5
Molecular Formula:C₄₃H₄₂NO₃P
Molecular Weight:651.785
Hs Code.:

<5-<Bis(4-methoxyphenyl)methyl>-3-tert-butyl-2-hydroxyphenylimino>triphenylphosphoran

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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 <5--3-tert-butyl-2-hydroxyphenylimino>triphenylphosphoran

Chemical Property:

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Technology Process of <5--3-tert-butyl-2-hydroxyphenylimino>triphenylphosphoran

There total 2 articles about <5--3-tert-butyl-2-hydroxyphenylimino>triphenylphosphoran 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: 62.0%

: 77464-20-1
2-Amino-4-[bis-(4-methoxy-phenyl)-methyl]-6-tert-butyl-phenol

: 1034-39-5
dibromotriphenylphosphorane

: 76826-04-5
<5--3-tert-butyl-2-hydroxyphenylimino>triphenylphosphoran

Guidance literature:

Reference yield:

: 77464-20-1
2-Amino-4-[bis-(4-methoxy-phenyl)-methyl]-6-tert-butyl-phenol

: 603-35-0
triphenylphosphine

: 76826-04-5
<5--3-tert-butyl-2-hydroxyphenylimino>triphenylphosphoran

Guidance literature:: With hexachloroethane; triethylamine; Yield given. Multistep reaction; 1.) CH₃CN, 1 h, reflux, 2.) benzene, 10 min, reflux;

Reference yield:

: 76826-04-5
<5--3-tert-butyl-2-hydroxyphenylimino>triphenylphosphoran

: 76826-16-9
5-[Bis-(4-methoxy-phenyl)-methyl]-7-tert-butyl-2,2,2-triphenyl-1-oxa-3-aza-2λ⁵-phospha-indan

Guidance literature:: Equilibrium constant; Thermodynamic data; Kinetics; 1,3,2-benzoxazaphospholine-tautomerism; ΔS, ΔH, ΔG, Ea, activation: ΔG, ΔH, ΔS;