2-(benzyl(tert-butoxycarbonyl)amino)-1-(4-methoxyphenyl)ethyl 4-fluorobenzenesulfonate

Base Information

Chemical Name:2-(benzyl(tert-butoxycarbonyl)amino)-1-(4-methoxyphenyl)ethyl 4-fluorobenzenesulfonate
CAS No.:1345986-09-5
Molecular Formula:C₂₇H₃₀FNO₆S
Molecular Weight:515.603
Hs Code.:

Synonyms:2-(benzyl(tert-butoxycarbonyl)amino)-1-(4-methoxyphenyl)ethyl 4-fluorobenzenesulfonate

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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 2-(benzyl(tert-butoxycarbonyl)amino)-1-(4-methoxyphenyl)ethyl 4-fluorobenzenesulfonate

Chemical Property:

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Technology Process of 2-(benzyl(tert-butoxycarbonyl)amino)-1-(4-methoxyphenyl)ethyl 4-fluorobenzenesulfonate

There total 9 articles about 2-(benzyl(tert-butoxycarbonyl)amino)-1-(4-methoxyphenyl)ethyl 4-fluorobenzenesulfonate 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: 73.0%

: 1345986-16-4
C₂₁H₂₇NO₄

: 349-88-2
4-Fluorobenzenesulfonyl chloride

: 1345986-09-5
2-(benzyl(tert-butoxycarbonyl)amino)-1-(4-methoxyphenyl)ethyl 4-fluorobenzenesulfonate

Guidance literature:: C₂₁H₂₇NO₄; With potassium hydroxide; In tetrahydrofuran; for 0.25h;

4-Fluorobenzenesulfonyl chloride; In tetrahydrofuran;
DOI:10.1016/j.bmcl.2011.08.078

Reference yield:

: 100-46-9
benzylamine

: 1345986-09-5
2-(benzyl(tert-butoxycarbonyl)amino)-1-(4-methoxyphenyl)ethyl 4-fluorobenzenesulfonate

Guidance literature:: Multi-step reaction with 3 steps

1: activated silica / 24 h / Inert atmosphere

2: triethylamine / methanol / 0.5 h / Reflux

3: potassium hydroxide / tetrahydrofuran / 0.25 h

With triethylamine; potassium hydroxide; In tetrahydrofuran; methanol;
DOI:10.1016/j.bmcl.2011.08.078

Reference yield:

: 6388-72-3
2-(4-methoxyphenyl)oxirane

: 1345986-09-5
2-(benzyl(tert-butoxycarbonyl)amino)-1-(4-methoxyphenyl)ethyl 4-fluorobenzenesulfonate

Guidance literature:: Multi-step reaction with 3 steps

1: activated silica / 24 h / Inert atmosphere

2: triethylamine / methanol / 0.5 h / Reflux

3: potassium hydroxide / tetrahydrofuran / 0.25 h

With triethylamine; potassium hydroxide; In tetrahydrofuran; methanol;
DOI:10.1016/j.bmcl.2011.08.078