tert-butyl benzyl(2-(methoxy(methyl)amino)-2-oxo-1-phenylethyl)carbamate

Base Information

Chemical Name:tert-butyl benzyl(2-(methoxy(methyl)amino)-2-oxo-1-phenylethyl)carbamate
CAS No.:1325715-42-1
Molecular Formula:C₂₂H₂₈N₂O₄
Molecular Weight:384.475
Hs Code.:

Synonyms:tert-butyl benzyl(2-(methoxy(methyl)amino)-2-oxo-1-phenylethyl)carbamate

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Chemical Property of tert-butyl benzyl(2-(methoxy(methyl)amino)-2-oxo-1-phenylethyl)carbamate

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Technology Process of tert-butyl benzyl(2-(methoxy(methyl)amino)-2-oxo-1-phenylethyl)carbamate

There total 6 articles about tert-butyl benzyl(2-(methoxy(methyl)amino)-2-oxo-1-phenylethyl)carbamate 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: 60.0%

: 6638-79-5
N,O-dimethylhydroxylamine*hydrochloride

: 2-(benzyl(tert-butoxycarbonyl)amino)-2-phenylacetic acid

: 1325715-42-1
tert-butyl benzyl(2-(methoxy(methyl)amino)-2-oxo-1-phenylethyl)carbamate

Guidance literature:: 2-(benzyl(tert-butoxycarbonyl)amino)-2-phenylacetic acid; With (benzotriazol-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; triethylamine; In dichloromethane; at 20 ℃; for 0.25h; Inert atmosphere;

N,O-dimethylhydroxylamine*hydrochloride; In dichloromethane; at 20 ℃; for 18h; Inert atmosphere;
DOI:10.1016/j.bmcl.2011.05.123

Reference yield:

: 2935-35-5
(S)-2-phenylglycine

: 1325715-42-1
tert-butyl benzyl(2-(methoxy(methyl)amino)-2-oxo-1-phenylethyl)carbamate

Guidance literature:: Multi-step reaction with 4 steps

1.1: lithium hydroxide monohydrate / methanol / 0.33 h / 20 °C

1.2: 1 h

2.1: sodium tetrahydroborate / methanol / 0.5 h

3.1: tetra(n-butyl)ammonium hydroxide / acetonitrile / 0.5 h / 20 °C

3.2: 18 h / 20 °C

4.1: (benzotriazol-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; triethylamine / dichloromethane / 0.25 h / 20 °C / Inert atmosphere

4.2: 18 h / 20 °C / Inert atmosphere

With sodium tetrahydroborate; (benzotriazol-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; lithium hydroxide monohydrate; tetra(n-butyl)ammonium hydroxide; triethylamine; In methanol; dichloromethane; acetonitrile;
DOI:10.1016/j.bmcl.2011.05.123

Reference yield:

: 24424-99-5
di-tert-butyl dicarbonate

: 1325715-42-1
tert-butyl benzyl(2-(methoxy(methyl)amino)-2-oxo-1-phenylethyl)carbamate

Guidance literature:: Multi-step reaction with 2 steps

1.1: tetra(n-butyl)ammonium hydroxide / acetonitrile / 0.5 h / 20 °C

1.2: 18 h / 20 °C

2.1: (benzotriazol-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; triethylamine / dichloromethane / 0.25 h / 20 °C / Inert atmosphere

2.2: 18 h / 20 °C / Inert atmosphere

With (benzotriazol-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; tetra(n-butyl)ammonium hydroxide; triethylamine; In dichloromethane; acetonitrile;
DOI:10.1016/j.bmcl.2011.05.123