bromo-acetic acid 3-(4-benzyloxycarbonyloxy-phenyl)-2-tert-butoxycarbonylamino-propyl ester

Base Information

Chemical Name:bromo-acetic acid 3-(4-benzyloxycarbonyloxy-phenyl)-2-tert-butoxycarbonylamino-propyl ester
CAS No.:256643-19-3
Molecular Formula:C₂₄H₂₈BrNO₇
Molecular Weight:522.393
Hs Code.:

bromo-acetic acid 3-(4-benzyloxycarbonyloxy-phenyl)-2-<i>tert</i>-butoxycarbonylamino-propyl ester

Synonyms:bromo-acetic acid 3-(4-benzyloxycarbonyloxy-phenyl)-2-tert-butoxycarbonylamino-propyl ester

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Chemical Property of bromo-acetic acid 3-(4-benzyloxycarbonyloxy-phenyl)-2-tert-butoxycarbonylamino-propyl ester

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Technology Process of bromo-acetic acid 3-(4-benzyloxycarbonyloxy-phenyl)-2-tert-butoxycarbonylamino-propyl ester

There total 3 articles about bromo-acetic acid 3-(4-benzyloxycarbonyloxy-phenyl)-2-tert-butoxycarbonylamino-propyl 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: 57.0%

: 598-21-0
2-Bromoacetyl bromide

: 256643-07-9
N-Boc-L-(OZ)tyrosinol

: 256643-19-3
bromo-acetic acid 3-(4-benzyloxycarbonyloxy-phenyl)-2-tert-butoxycarbonylamino-propyl ester

Guidance literature:: With N,N-dimethyl-aniline; In dichloromethane; at 20 ℃; for 1h;
DOI:10.1016/S0968-0896(99)00192-3

Reference yield:

: 501-53-1,94274-21-2
benzyl chloroformate

: 256643-19-3
bromo-acetic acid 3-(4-benzyloxycarbonyloxy-phenyl)-2-tert-butoxycarbonylamino-propyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 56 percent / Et₃N / CH₂Cl₂ / 1 h / 20 °C

2: 57 percent / N,N-dimethylaniline / CH₂Cl₂ / 1 h / 20 °C

With N,N-dimethyl-aniline; triethylamine; In dichloromethane; 1: Acylation / 2: Esterification;
DOI:10.1016/S0968-0896(99)00192-3

Reference yield:

: 83345-46-4,282100-80-5
N-(tert-butyloxycarbonyl)-L-tyrosinol

: 256643-19-3
bromo-acetic acid 3-(4-benzyloxycarbonyloxy-phenyl)-2-tert-butoxycarbonylamino-propyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 56 percent / Et₃N / CH₂Cl₂ / 1 h / 20 °C

2: 57 percent / N,N-dimethylaniline / CH₂Cl₂ / 1 h / 20 °C

With N,N-dimethyl-aniline; triethylamine; In dichloromethane; 1: Acylation / 2: Esterification;
DOI:10.1016/S0968-0896(99)00192-3