{2-[(benzyloxy-tert-butyloxycarbonyl-amino)-methyl]-phenyl}-phosphonic acid diethyl ester

Base Information

Chemical Name:{2-[(benzyloxy-tert-butyloxycarbonyl-amino)-methyl]-phenyl}-phosphonic acid diethyl ester
CAS No.:950846-93-2
Molecular Formula:C₂₃H₃₂NO₆P
Molecular Weight:449.484
Hs Code.:

Synonyms:{2-[(benzyloxy-tert-butyloxycarbonyl-amino)-methyl]-phenyl}-phosphonic acid diethyl ester

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Chemical Property of {2-[(benzyloxy-tert-butyloxycarbonyl-amino)-methyl]-phenyl}-phosphonic acid diethyl ester

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Technology Process of {2-[(benzyloxy-tert-butyloxycarbonyl-amino)-methyl]-phenyl}-phosphonic acid diethyl ester

There total 1 articles about {2-[(benzyloxy-tert-butyloxycarbonyl-amino)-methyl]-phenyl}-phosphonic acid diethyl 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: 72.0%

: 75777-37-6
(2-bromomethyl-phenyl)-phosphonic acid diethyl ester

: 79722-21-7
tert-butyl N-(benzyloxy)carbamate

: 950846-93-2
{2-[(benzyloxy-tert-butyloxycarbonyl-amino)-methyl]-phenyl}-phosphonic acid diethyl ester

Guidance literature:: tert-butyl N-(benzyloxy)carbamate; With sodium hydride; In tetrahydrofuran; at 0 - 5 ℃;

(2-bromomethyl-phenyl)-phosphonic acid diethyl ester; With sodium iodide; In tetrahydrofuran; at 20 ℃; Further stages.;
DOI:10.1002/ardp.200700013

Reference yield:

: 950846-93-2
{2-[(benzyloxy-tert-butyloxycarbonyl-amino)-methyl]-phenyl}-phosphonic acid diethyl ester

: 2,2-dimethyl-propionic acid (2,2-dimethyl-propionyloxymethoxy)-{2-[(formyl-hydroxy-amino)-methyl]-phenyl}-phosphinoyloxymethyl ester

Guidance literature:: Multi-step reaction with 5 steps

1.1: 92 percent / trifluoroacetic acid / CH₂Cl₂ / 1 h / 20 °C

2.1: Ac₂O / 0.5 h / 20 °C

2.2: 97 percent / 0 - 20 °C

3.1: trimethylsilyl bromide / CH₂Cl₂ / 24 h / 20 °C

3.2: water / tetrahydrofuran / 0.17 h / 20 °C

4.1: Et₃N / dimethylformamide / 6 h / 70 °C

5.1: 81 percent / H₂ / Pd/C / methanol / 2 h / 1500.15 Torr

With trimethylsilyl bromide; hydrogen; acetic anhydride; triethylamine; trifluoroacetic acid; palladium on activated charcoal; In methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1002/ardp.200700013

Reference yield:

: 950846-93-2
{2-[(benzyloxy-tert-butyloxycarbonyl-amino)-methyl]-phenyl}-phosphonic acid diethyl ester

: 2,2-dimethyl-propionic acid {2-[(acetyl-hydroxy-amino)-methyl]-phenyl}-(2,2-dimethyl-propionyloxymethoxy)-phosphinoyloxymethyl ester

Guidance literature:: Multi-step reaction with 5 steps

1.1: 92 percent / trifluoroacetic acid / CH₂Cl₂ / 1 h / 20 °C

2.1: 98 percent / Et₃N / CH₂Cl₂ / 2 h / 20 °C

3.1: trimethylsilyl bromide / CH₂Cl₂ / 24 h / 20 °C

3.2: water / tetrahydrofuran / 0.17 h / 20 °C

4.1: Et₃N / dimethylformamide / 6 h / 70 °C

5.1: 79 percent / H₂ / Pd/C / methanol / 2 h / 1500.15 Torr

With trimethylsilyl bromide; hydrogen; triethylamine; trifluoroacetic acid; palladium on activated charcoal; In methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1002/ardp.200700013