(S)-tert-butyl 2,2,2-trifluoro-1-(2-((4-methoxyphenyl)ethynyl)phenyl)ethylcarbamate

Base Information

Chemical Name:(S)-tert-butyl 2,2,2-trifluoro-1-(2-((4-methoxyphenyl)ethynyl)phenyl)ethylcarbamate
CAS No.:1421615-56-6
Molecular Formula:C₂₂H₂₂F₃NO₃
Molecular Weight:405.417
Hs Code.:

Synonyms:(S)-tert-butyl 2,2,2-trifluoro-1-(2-((4-methoxyphenyl)ethynyl)phenyl)ethylcarbamate

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Chemical Property of (S)-tert-butyl 2,2,2-trifluoro-1-(2-((4-methoxyphenyl)ethynyl)phenyl)ethylcarbamate

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Technology Process of (S)-tert-butyl 2,2,2-trifluoro-1-(2-((4-methoxyphenyl)ethynyl)phenyl)ethylcarbamate

There total 5 articles about (S)-tert-butyl 2,2,2-trifluoro-1-(2-((4-methoxyphenyl)ethynyl)phenyl)ethylcarbamate 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: 93.0%

: 1421615-46-4
(S)-tert-butyl [2,2,2-trifluoro-1-(2-iodophenyl)ethyl]carbamate

: 768-60-5
4-methoxyphenylacetylen

: 1421615-56-6
(S)-tert-butyl 2,2,2-trifluoro-1-(2-((4-methoxyphenyl)ethynyl)phenyl)ethylcarbamate

Guidance literature:: (S)-tert-butyl [2,2,2-trifluoro-1-(2-iodophenyl)ethyl]carbamate; 4-methoxyphenylacetylen; With bis-triphenylphosphine-palladium(II) chloride; triethylamine; In tetrahydrofuran; at 20 ℃; for 0.166667h; Inert atmosphere;

With copper(l) iodide; In tetrahydrofuran; for 6h; Inert atmosphere; Heating;
DOI:10.1021/ol3035142

Reference yield:

: (S)-(+)-N-(2-iodobenzylidene)-2-methylpropane-2-sulfinamide

: 1421615-56-6
(S)-tert-butyl 2,2,2-trifluoro-1-(2-((4-methoxyphenyl)ethynyl)phenyl)ethylcarbamate

Guidance literature:: Multi-step reaction with 4 steps

1.1: tetrabutylammonium acetate / tetrahydrofuran / -20 °C / Inert atmosphere

2.1: hydrogenchloride / 1,4-dioxane; methanol / 0.33 h / 20 °C / Inert atmosphere

3.1: potassium carbonate / 1,4-dioxane / 20 °C / Inert atmosphere

4.1: bis-triphenylphosphine-palladium(II) chloride; triethylamine / tetrahydrofuran / 0.17 h / 20 °C / Inert atmosphere

4.2: 6 h / Inert atmosphere; Heating

With hydrogenchloride; bis-triphenylphosphine-palladium(II) chloride; tetrabutylammonium acetate; potassium carbonate; triethylamine; In tetrahydrofuran; 1,4-dioxane; methanol; 4.2: |Sonogashira Cross-Coupling;
DOI:10.1021/ol3035142

Reference yield:

: 1421615-37-3
(R)-2-methyl-N-[(S)-2,2,2-trifluoro-1-(2-iodophenyl)ethyl]propane-2-sulfinamide

: 1421615-56-6
(S)-tert-butyl 2,2,2-trifluoro-1-(2-((4-methoxyphenyl)ethynyl)phenyl)ethylcarbamate

Guidance literature:: Multi-step reaction with 3 steps

1.1: hydrogenchloride / 1,4-dioxane; methanol / 0.33 h / 20 °C / Inert atmosphere

2.1: potassium carbonate / 1,4-dioxane / 20 °C / Inert atmosphere

3.1: bis-triphenylphosphine-palladium(II) chloride; triethylamine / tetrahydrofuran / 0.17 h / 20 °C / Inert atmosphere

3.2: 6 h / Inert atmosphere; Heating

With hydrogenchloride; bis-triphenylphosphine-palladium(II) chloride; potassium carbonate; triethylamine; In tetrahydrofuran; 1,4-dioxane; methanol; 3.2: |Sonogashira Cross-Coupling;
DOI:10.1021/ol3035142