[(2-amino-5-chlorobenzyl)-tert-butoxycarbonylamino]acetic acid ethyl ester

Base Information

Chemical Name:[(2-amino-5-chlorobenzyl)-tert-butoxycarbonylamino]acetic acid ethyl ester
CAS No.:1226807-99-3
Molecular Formula:C₁₆H₂₃ClN₂O₄
Molecular Weight:342.823
Hs Code.:

Synonyms:[(2-amino-5-chlorobenzyl)-tert-butoxycarbonylamino]acetic acid ethyl ester

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Chemical Property of [(2-amino-5-chlorobenzyl)-tert-butoxycarbonylamino]acetic acid ethyl ester

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Technology Process of [(2-amino-5-chlorobenzyl)-tert-butoxycarbonylamino]acetic acid ethyl ester

There total 4 articles about [(2-amino-5-chlorobenzyl)-tert-butoxycarbonylamino]acetic acid ethyl ester 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: 95.5%

: 1226807-98-2
[tert-butoxycarbonyl-(5-chloro-2-nitrobenzyl)amino]acetic acid ethyl ester

: 1226807-99-3
[(2-amino-5-chlorobenzyl)-tert-butoxycarbonylamino]acetic acid ethyl ester

Guidance literature:: With hydrogen; zinc dibromide; palladium 10% on activated carbon; In ethyl acetate; for 48h; Inert atmosphere;

Reference yield:

: 50608-35-0
(5-chloro-2-nitrobenzylamino)acetic acid ethyl ester

: 1226807-99-3
[(2-amino-5-chlorobenzyl)-tert-butoxycarbonylamino]acetic acid ethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: dmap / dichloromethane / 18 h / 0 - 20 °C

2: hydrogen; zinc dibromide / palladium 10% on activated carbon / ethyl acetate / 48 h / 20 °C

With dmap; hydrogen; zinc dibromide; palladium 10% on activated carbon; In dichloromethane; ethyl acetate;

Reference yield:

: 73033-58-6
5-chloro-2-nitrobenzyl alcohol

: 1226807-99-3
[(2-amino-5-chlorobenzyl)-tert-butoxycarbonylamino]acetic acid ethyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: thionyl chloride; triethylamine / dichloromethane / 3.5 h / 32 °C

2: triethylamine / 8 h / Reflux

3: dmap / dichloromethane / 18 h / 0 - 20 °C

4: hydrogen; zinc dibromide / palladium 10% on activated carbon / ethyl acetate / 48 h / 20 °C

With dmap; thionyl chloride; hydrogen; triethylamine; zinc dibromide; palladium 10% on activated carbon; In dichloromethane; ethyl acetate;