3-benzoylimino-1-methyl-2-(4-nitrophenyl)-2,3,5,6-tetrahydrobenzoindolizin-2-ol

Base Information

Chemical Name:3-benzoylimino-1-methyl-2-(4-nitrophenyl)-2,3,5,6-tetrahydrobenzoindolizin-2-ol
CAS No.:91417-02-6
Molecular Formula:C₂₆H₂₁N₃O₄
Molecular Weight:439.47
Hs Code.:

3-benzoylimino-1-methyl-2-(4-nitrophenyl)-2,3,5,6-tetrahydrobenzo<g>indolizin-2-ol

Synonyms:3-benzoylimino-1-methyl-2-(4-nitrophenyl)-2,3,5,6-tetrahydrobenzoindolizin-2-ol

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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-benzoylimino-1-methyl-2-(4-nitrophenyl)-2,3,5,6-tetrahydrobenzoindolizin-2-ol

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Technology Process of 3-benzoylimino-1-methyl-2-(4-nitrophenyl)-2,3,5,6-tetrahydrobenzoindolizin-2-ol

There total 3 articles about 3-benzoylimino-1-methyl-2-(4-nitrophenyl)-2,3,5,6-tetrahydrobenzoindolizin-2-ol 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: 84.0%

: 98-88-4
benzoyl chloride

: 91417-05-9
3-imino-1-methyl-2-(4-nitrophenyl)-2,3,5,6-tetrahydrobenzoindolizin-2-ol

: 91417-02-6
3-benzoylimino-1-methyl-2-(4-nitrophenyl)-2,3,5,6-tetrahydrobenzoindolizin-2-ol

Guidance literature:: With sodium hydrogencarbonate; In diethyl ether; water;

Reference yield:

: 41173-70-0
1-ethyl-3,4-dihydro-isoquinoline

: 91417-02-6
3-benzoylimino-1-methyl-2-(4-nitrophenyl)-2,3,5,6-tetrahydrobenzoindolizin-2-ol

Guidance literature:: Multi-step reaction with 2 steps

1: 49 percent / benzene / 4 h / Ambient temperature

2: 84 percent / 10percent sodium bicarbonate / diethyl ether; H₂O

With sodium hydrogencarbonate; In diethyl ether; water; benzene;

Reference yield:

: 6048-20-0
4-nitrobenzoyl cyanide

: 91417-02-6
3-benzoylimino-1-methyl-2-(4-nitrophenyl)-2,3,5,6-tetrahydrobenzoindolizin-2-ol

Guidance literature:: Multi-step reaction with 2 steps

1: 49 percent / benzene / 4 h / Ambient temperature

2: 84 percent / 10percent sodium bicarbonate / diethyl ether; H₂O

With sodium hydrogencarbonate; In diethyl ether; water; benzene;