tert-butyl 2-(4-(5-(1-((benzylcarbamoyl)oxy)propyl)isoxazol-3-yl)phenoxy)-2-methylpropanoate

Base Information

Chemical Name:tert-butyl 2-(4-(5-(1-((benzylcarbamoyl)oxy)propyl)isoxazol-3-yl)phenoxy)-2-methylpropanoate
CAS No.:1621513-93-6
Molecular Formula:C₂₈H₃₄N₂O₆
Molecular Weight:494.588
Hs Code.:

Synonyms:tert-butyl 2-(4-(5-(1-((benzylcarbamoyl)oxy)propyl)isoxazol-3-yl)phenoxy)-2-methylpropanoate

Suppliers and Price of tert-butyl 2-(4-(5-(1-((benzylcarbamoyl)oxy)propyl)isoxazol-3-yl)phenoxy)-2-methylpropanoate

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Total 1 raw suppliers

Chemical Property of tert-butyl 2-(4-(5-(1-((benzylcarbamoyl)oxy)propyl)isoxazol-3-yl)phenoxy)-2-methylpropanoate

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

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Technology Process of tert-butyl 2-(4-(5-(1-((benzylcarbamoyl)oxy)propyl)isoxazol-3-yl)phenoxy)-2-methylpropanoate

There total 5 articles about tert-butyl 2-(4-(5-(1-((benzylcarbamoyl)oxy)propyl)isoxazol-3-yl)phenoxy)-2-methylpropanoate 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: 99.0%

: 1621513-92-5
tert-butyl 2-(4-(5-(1-hydroxypropyl)isoxazol-3-yl)phenoxy)-2-methylpropanoate

: 3173-56-6
benzyl isothiocyanate

: 1621513-93-6
tert-butyl 2-(4-(5-(1-((benzylcarbamoyl)oxy)propyl)isoxazol-3-yl)phenoxy)-2-methylpropanoate

Guidance literature:: With pyridine; copper(l) chloride; In dichloromethane; at 20 ℃; for 2h; Inert atmosphere;
DOI:10.1002/anie.201310618

Reference yield:

: 23877-12-5
tert-butyl bromoisobutyrate

: 1621513-93-6
tert-butyl 2-(4-(5-(1-((benzylcarbamoyl)oxy)propyl)isoxazol-3-yl)phenoxy)-2-methylpropanoate

Guidance literature:: Multi-step reaction with 4 steps

1: potassium carbonate; magnesium sulfate / N,N-dimethyl-formamide / Inert atmosphere

2: hydroxylamine hydrochloride; sodium carbonate / ethanol; water / 12 h / 65 °C / Inert atmosphere

3: N-chloro-succinimide; pyridine; triethylamine / tetrahydrofuran / 1 h / 60 °C / Inert atmosphere

4: pyridine; copper(l) chloride / dichloromethane / 2 h / 20 °C / Inert atmosphere

With pyridine; N-chloro-succinimide; hydroxylamine hydrochloride; sodium carbonate; magnesium sulfate; potassium carbonate; triethylamine; copper(l) chloride; In tetrahydrofuran; ethanol; dichloromethane; water; N,N-dimethyl-formamide;
DOI:10.1002/anie.201310618

Reference yield:

: 343322-79-2
tert-butyl 2-(4-formylphenoxy)-2-methylpropanoate

: 1621513-93-6
tert-butyl 2-(4-(5-(1-((benzylcarbamoyl)oxy)propyl)isoxazol-3-yl)phenoxy)-2-methylpropanoate

Guidance literature:: Multi-step reaction with 3 steps

1: hydroxylamine hydrochloride; sodium carbonate / ethanol; water / 12 h / 65 °C / Inert atmosphere

2: N-chloro-succinimide; pyridine; triethylamine / tetrahydrofuran / 1 h / 60 °C / Inert atmosphere

3: pyridine; copper(l) chloride / dichloromethane / 2 h / 20 °C / Inert atmosphere

With pyridine; N-chloro-succinimide; hydroxylamine hydrochloride; sodium carbonate; triethylamine; copper(l) chloride; In tetrahydrofuran; ethanol; dichloromethane; water;
DOI:10.1002/anie.201310618