[3-methoxy-N-(3-oxopropyl)-N-phenylcyclohexa-1,3-dienecarboxamide]tricarbonyl iron

Base Information

Chemical Name:[3-methoxy-N-(3-oxopropyl)-N-phenylcyclohexa-1,3-dienecarboxamide]tricarbonyl iron
CAS No.:1400786-10-8
Molecular Formula:C₂₀H₁₉FeNO₆
Molecular Weight:425.221
Hs Code.:

Synonyms:[3-methoxy-N-(3-oxopropyl)-N-phenylcyclohexa-1,3-dienecarboxamide]tricarbonyl iron

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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 [3-methoxy-N-(3-oxopropyl)-N-phenylcyclohexa-1,3-dienecarboxamide]tricarbonyl iron

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Technology Process of [3-methoxy-N-(3-oxopropyl)-N-phenylcyclohexa-1,3-dienecarboxamide]tricarbonyl iron

There total 1 articles about [3-methoxy-N-(3-oxopropyl)-N-phenylcyclohexa-1,3-dienecarboxamide]tricarbonyl iron 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: 94.0%

: 1400786-09-5
[3-methoxy-N-(3-methoxyallyl)-N-phenylcyclohexa-1,3-dienecarboxamide]tricarbonyl iron

: 1400786-10-8
[3-methoxy-N-(3-oxopropyl)-N-phenylcyclohexa-1,3-dienecarboxamide]tricarbonyl iron

Guidance literature:: With hydrogenchloride; In 1,4-dioxane; water; at 20 ℃; for 1.5h;
DOI:10.1021/jo301721d

Reference yield:

: 1027156-11-1
tert-butyldimethylsilyl 2-methylpropane-2-sulfonate

: 1400786-10-8
[3-methoxy-N-(3-oxopropyl)-N-phenylcyclohexa-1,3-dienecarboxamide]tricarbonyl iron

: 1400786-12-0
[N-(3-((tert-butyldimethylsilyl)oxy)allyl)-3-methoxy-N-phenylcyclohexa-1,3-dienecarboxamide]tricarbonyl iron

: 1400786-12-0
[N-(3-((tert-butyldimethylsilyl)oxy)allyl)-3-methoxy-N-phenylcyclohexa-1,3-dienecarboxamide]tricarbonyl iron

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 0 ℃; for 2h; Overall yield = 80 %; Overall yield = 39.3 mg; Inert atmosphere;
DOI:10.1021/jo301721d