N-ferrocenylidenediphenylmethylamine

Base Information

Chemical Name:N-ferrocenylidenediphenylmethylamine
CAS No.:376392-83-5
Molecular Formula:C₂₄H₂₁FeN
Molecular Weight:379.284
Hs Code.:

Synonyms:

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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 N-ferrocenylidenediphenylmethylamine

Chemical Property:

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Technology Process of N-ferrocenylidenediphenylmethylamine

There total 1 articles about N-ferrocenylidenediphenylmethylamine 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: 90.0%

: 12093-10-6
ferrocenecarboxaldehyde

: 91-00-9
Benzhydrylamine

: 376392-83-5
N-ferrocenylidenediphenylmethylamine

Guidance literature:: In methanol; the mixt. in methanol was stirred for 20 h at room temp.; evapd., the solid was dissolved in benzene and pptd. with hexane; elem. anal.;
DOI:10.1016/S0022-328X(01)01011-7

Reference yield: 75.0%

: 376392-83-5
N-ferrocenylidenediphenylmethylamine

: 762-04-9
phosphonic acid diethyl ester

: diethyl N-diphenylmethylamino(ferrocenyl)methanephosphonate

Guidance literature:: In toluene; the mixt. in toluene was refluxed for 7 h then stirred at room temp. for12 h; evapd., dissolved in 10% aq. HCl-ethanol, washed with ether, the aq. layer was extd. with CH2Cl2, the organic layer dried and evapd., column chromy. on cellulose powder; elem. anal.;
DOI:10.1016/S0022-328X(01)01011-7

Reference yield: 72.0%

: 376392-83-5
N-ferrocenylidenediphenylmethylamine

: 17176-77-1
Dibenzyl phosphite

: dibenzyl N-diphenylmethylamino(ferrocenyl)methanephosphonate

Guidance literature:: In toluene; the mixt. in toluene was refluxed for 7 h then stirred at room temp. for12 h; evapd., dissolved in 10% aq. HCl-ethanol, washed with ether, the aq. layer was extd. with CH2Cl2, the organic layer dried and evapd., column chromy. on cellulose powder; elem. anal.;
DOI:10.1016/S0022-328X(01)01011-7