5-(2-benzylsulfanyl-2-(4-bromophenyl)ethyl)-3-methyl-4-nitroisoxazole

Base Information

Chemical Name:5-(2-benzylsulfanyl-2-(4-bromophenyl)ethyl)-3-methyl-4-nitroisoxazole
CAS No.:1314231-01-0
Molecular Formula:C₁₉H₁₇BrN₂O₃S
Molecular Weight:433.326
Hs Code.:

Synonyms:5-(2-benzylsulfanyl-2-(4-bromophenyl)ethyl)-3-methyl-4-nitroisoxazole

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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-(2-benzylsulfanyl-2-(4-bromophenyl)ethyl)-3-methyl-4-nitroisoxazole

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Technology Process of 5-(2-benzylsulfanyl-2-(4-bromophenyl)ethyl)-3-methyl-4-nitroisoxazole

There total 2 articles about 5-(2-benzylsulfanyl-2-(4-bromophenyl)ethyl)-3-methyl-4-nitroisoxazole 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%

: 86453-96-5,117504-15-1
3-methyl-4-nitro-5-(4-bromostyryl)isoxazole

: 100-53-8
phenylmethanethiol

: 1314231-01-0
5-(2-benzylsulfanyl-2-(4-bromophenyl)ethyl)-3-methyl-4-nitroisoxazole

Guidance literature:: With piperidine; In acetonitrile; at 20 ℃;
DOI:10.1016/j.tetlet.2011.05.007

Reference yield:

: 1123-49-5
3,5-dimethyl-4-nitroisoxazole

: 1122-91-4
4-bromo-benzaldehyde

: 1314231-01-0
5-(2-benzylsulfanyl-2-(4-bromophenyl)ethyl)-3-methyl-4-nitroisoxazole

Guidance literature:: Multi-step reaction with 2 steps

1: piperidine / acetonitrile / 4 h / Reflux

2: piperidine / acetonitrile / 20 °C

With piperidine; In acetonitrile; 1: Knoevenagel condensation / 2: Michael reaction;
DOI:10.1016/j.tetlet.2011.05.007