(R)-methyl 2-((2-((tert-butoxycarbonyl)amino)-3-phenylpropyl)thio)benzoate

Base Information

Chemical Name:(R)-methyl 2-((2-((tert-butoxycarbonyl)amino)-3-phenylpropyl)thio)benzoate
CAS No.:153923-48-9
Molecular Formula:C₂₂H₂₇NO₄S
Molecular Weight:401.527
Hs Code.:

Synonyms:(R)-methyl 2-((2-((tert-butoxycarbonyl)amino)-3-phenylpropyl)thio)benzoate

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Chemical Property of (R)-methyl 2-((2-((tert-butoxycarbonyl)amino)-3-phenylpropyl)thio)benzoate

Chemical Property:

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Technology Process of (R)-methyl 2-((2-((tert-butoxycarbonyl)amino)-3-phenylpropyl)thio)benzoate

There total 5 articles about (R)-methyl 2-((2-((tert-butoxycarbonyl)amino)-3-phenylpropyl)thio)benzoate 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: 86.0%

: 141595-88-2
(R)-tert-butyl (1-bromo-3-phenylpropan-2-yl)carbamate

: 4892-02-8
Methyl thiosalicylate

: 153923-48-9
(R)-methyl 2-((2-((tert-butoxycarbonyl)amino)-3-phenylpropyl)thio)benzoate

Guidance literature:: Methyl thiosalicylate; With potassium carbonate; In N,N-dimethyl-formamide; at 20 ℃; for 0.166667h;

(R)-tert-butyl (1-bromo-3-phenylpropan-2-yl)carbamate; In N,N-dimethyl-formamide; at 60 ℃; for 4h;

Reference yield:

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

: 153923-48-9
(R)-methyl 2-((2-((tert-butoxycarbonyl)amino)-3-phenylpropyl)thio)benzoate

Guidance literature:: Multi-step reaction with 3 steps

1.1: dichloromethane / 0 - 20 °C

2.1: triphenylphosphine; carbon tetrabromide / dichloromethane / 0 - 20 °C / Inert atmosphere

3.1: potassium carbonate / N,N-dimethyl-formamide / 0.17 h / 20 °C

3.2: 4 h / 60 °C

With carbon tetrabromide; potassium carbonate; triphenylphosphine; In dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 106454-69-7
N-tert-butoxycarbonyl-D-Phenylalaninol

: 153923-48-9
(R)-methyl 2-((2-((tert-butoxycarbonyl)amino)-3-phenylpropyl)thio)benzoate

Guidance literature:: Multi-step reaction with 2 steps

1.1: triphenylphosphine; carbon tetrabromide / dichloromethane / 0 - 20 °C / Inert atmosphere

2.1: potassium carbonate / N,N-dimethyl-formamide / 0.17 h / 20 °C

2.2: 4 h / 60 °C

With carbon tetrabromide; potassium carbonate; triphenylphosphine; In dichloromethane; N,N-dimethyl-formamide;