Methyl 3-chloro-4-<<5-(3-methyl-5-isoxazolyl)pentyl>oxy>-5-nitrobenzoate

Base Information

Chemical Name:Methyl 3-chloro-4-<<5-(3-methyl-5-isoxazolyl)pentyl>oxy>-5-nitrobenzoate
CAS No.:107356-05-8
Molecular Formula:C₁₇H₁₉ClN₂O₆
Molecular Weight:382.801
Hs Code.:

Synonyms:Methyl 3-chloro-4-<<5-(3-methyl-5-isoxazolyl)pentyl>oxy>-5-nitrobenzoate

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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 Methyl 3-chloro-4-<<5-(3-methyl-5-isoxazolyl)pentyl>oxy>-5-nitrobenzoate

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Technology Process of Methyl 3-chloro-4-<<5-(3-methyl-5-isoxazolyl)pentyl>oxy>-5-nitrobenzoate

There total 3 articles about Methyl 3-chloro-4-<<5-(3-methyl-5-isoxazolyl)pentyl>oxy>-5-nitrobenzoate 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: 78.0%

: 118276-21-4
3-Methyl-5-(5-hydroxypentyl)isoxazole

: 40256-81-3
Methyl 3-chloro-4-hydroxy-5-nitrobenzoate

: 107356-05-8
Methyl 3-chloro-4-<<5-(3-methyl-5-isoxazolyl)pentyl>oxy>-5-nitrobenzoate

Guidance literature:: With triphenylphosphine; diethylazodicarboxylate; In dichloromethane; Ambient temperature;
DOI:10.1021/jm00122a027

Reference yield:

: 98033-85-3
5-(5-bromopentyl)-3-methylisoxazole

: 107356-05-8
Methyl 3-chloro-4-<<5-(3-methyl-5-isoxazolyl)pentyl>oxy>-5-nitrobenzoate

Guidance literature:: Multi-step reaction with 2 steps

1: 57 percent / Amberlyst A-26 (carbonate form) / benzene / 4 h / Heating

2: 78 percent / triphenylphosphine, diethyl azodicarboxylate / CH₂Cl₂ / Ambient temperature

With Amberlyst A-26 (carbonate form); triphenylphosphine; diethylazodicarboxylate; In dichloromethane; benzene;
DOI:10.1021/jm00122a027