3-[4-(2-tert-butylphenoxymethyl)phenyl]isoxazole-5-carboxylic acid amide

Base Information

Chemical Name:3-[4-(2-tert-butylphenoxymethyl)phenyl]isoxazole-5-carboxylic acid amide
CAS No.:1613166-07-6
Molecular Formula:C₂₁H₂₂N₂O₃
Molecular Weight:350.417
Hs Code.:

Synonyms:3-[4-(2-tert-butylphenoxymethyl)phenyl]isoxazole-5-carboxylic acid amide

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Chemical Property of 3-[4-(2-tert-butylphenoxymethyl)phenyl]isoxazole-5-carboxylic acid amide

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Technology Process of 3-[4-(2-tert-butylphenoxymethyl)phenyl]isoxazole-5-carboxylic acid amide

There total 3 articles about 3-[4-(2-tert-butylphenoxymethyl)phenyl]isoxazole-5-carboxylic acid amide 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: 75.0%

: 88-18-6
2-tert-Butylphenol

: 1613166-38-3
3-(4-bromomethylphenyl)isoxazole-5-carboxylic acid amide

: 1613166-07-6
3-[4-(2-tert-butylphenoxymethyl)phenyl]isoxazole-5-carboxylic acid amide

Guidance literature:: With potassium carbonate; In acetonitrile; at 90 ℃; for 16h;

Reference yield:

: 1349734-64-0
4-bromomethylbenzaldehyde oxime

: 1613166-07-6
3-[4-(2-tert-butylphenoxymethyl)phenyl]isoxazole-5-carboxylic acid amide

Guidance literature:: Multi-step reaction with 3 steps

1: N-chloro-succinimide / N,N-dimethyl-formamide / 2 h / 20 °C / Inert atmosphere

2: sodium L-ascorbate; copper(II) sulfate; potassium hydrogencarbonate / water; tert-butyl alcohol / 3 h / 20 °C

3: potassium carbonate / acetonitrile / 16 h / 90 °C

With N-chloro-succinimide; potassium carbonate; potassium hydrogencarbonate; copper(II) sulfate; sodium L-ascorbate; In water; N,N-dimethyl-formamide; acetonitrile; tert-butyl alcohol;

Reference yield:

: 1349734-67-3
4-(bromomethyl)-N-hydroxybenzimidoyl chloride

: 1613166-07-6
3-[4-(2-tert-butylphenoxymethyl)phenyl]isoxazole-5-carboxylic acid amide

Guidance literature:: Multi-step reaction with 2 steps

1: sodium L-ascorbate; copper(II) sulfate; potassium hydrogencarbonate / water; tert-butyl alcohol / 3 h / 20 °C

2: potassium carbonate / acetonitrile / 16 h / 90 °C

With potassium carbonate; potassium hydrogencarbonate; copper(II) sulfate; sodium L-ascorbate; In water; acetonitrile; tert-butyl alcohol;