(S)-tert-Butyl (pyridin-2-yl(4-(trifluoromethyl)phenyl)methyl)-carbamate 2,2,2-trifluoroacetate

Base Information

Chemical Name:(S)-tert-Butyl (pyridin-2-yl(4-(trifluoromethyl)phenyl)methyl)-carbamate 2,2,2-trifluoroacetate
CAS No.:1416946-14-9
Molecular Formula:C₂HF₃O₂*C₁₈H₁₉F₃N₂O₂
Molecular Weight:466.38
Hs Code.:

Synonyms:(S)-tert-Butyl (pyridin-2-yl(4-(trifluoromethyl)phenyl)methyl)-carbamate 2,2,2-trifluoroacetate

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Chemical Property of (S)-tert-Butyl (pyridin-2-yl(4-(trifluoromethyl)phenyl)methyl)-carbamate 2,2,2-trifluoroacetate

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Technology Process of (S)-tert-Butyl (pyridin-2-yl(4-(trifluoromethyl)phenyl)methyl)-carbamate 2,2,2-trifluoroacetate

There total 5 articles about (S)-tert-Butyl (pyridin-2-yl(4-(trifluoromethyl)phenyl)methyl)-carbamate 2,2,2-trifluoroacetate 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:

: 405174-97-2
3-bromopicolinaldehyde

: 1416946-14-9
(S)-tert-Butyl (pyridin-2-yl(4-(trifluoromethyl)phenyl)methyl)-carbamate 2,2,2-trifluoroacetate

Guidance literature:: Multi-step reaction with 4 steps

1.1: copper(II) sulfate / dichloromethane / 20 °C

2.1: magnesium / tetrahydrofuran / 4 h

2.2: 1 h / -78 °C

3.1: hydrogenchloride / dichloromethane; 1,4-dioxane; ethanol / 2 h / 0 °C

3.2: 20 °C

4.1: tert.-butyl lithium / pentane; tetrahydrofuran / 0.18 h / 20 °C / Cooling with acetone-dry ice

With hydrogenchloride; tert.-butyl lithium; copper(II) sulfate; magnesium; In tetrahydrofuran; 1,4-dioxane; ethanol; dichloromethane; pentane;

Reference yield:

: 38749-79-0
3-bromo-2-picoline

: 1416946-14-9
(S)-tert-Butyl (pyridin-2-yl(4-(trifluoromethyl)phenyl)methyl)-carbamate 2,2,2-trifluoroacetate

Guidance literature:: Multi-step reaction with 6 steps

1.1: dibenzoyl peroxide; N-Bromosuccinimide / tetrachloromethane / 30 h / Reflux

2.1: morpholine / 1 h / 60 °C

2.2: pH 4

3.1: copper(II) sulfate / dichloromethane / 20 °C

4.1: magnesium / tetrahydrofuran / 4 h

4.2: 1 h / -78 °C

5.1: hydrogenchloride / dichloromethane; 1,4-dioxane; ethanol / 2 h / 0 °C

5.2: 20 °C

6.1: tert.-butyl lithium / pentane; tetrahydrofuran / 0.18 h / 20 °C / Cooling with acetone-dry ice

With morpholine; hydrogenchloride; N-Bromosuccinimide; tert.-butyl lithium; copper(II) sulfate; magnesium; dibenzoyl peroxide; In tetrahydrofuran; 1,4-dioxane; tetrachloromethane; ethanol; dichloromethane; pentane;

Reference yield:

: 3-bromo-2-(dibromomethyl)pyridine

: 1416946-14-9
(S)-tert-Butyl (pyridin-2-yl(4-(trifluoromethyl)phenyl)methyl)-carbamate 2,2,2-trifluoroacetate

Guidance literature:: Multi-step reaction with 5 steps

1.1: morpholine / 1 h / 60 °C

1.2: pH 4

2.1: copper(II) sulfate / dichloromethane / 20 °C

3.1: magnesium / tetrahydrofuran / 4 h

3.2: 1 h / -78 °C

4.1: hydrogenchloride / dichloromethane; 1,4-dioxane; ethanol / 2 h / 0 °C

4.2: 20 °C

5.1: tert.-butyl lithium / pentane; tetrahydrofuran / 0.18 h / 20 °C / Cooling with acetone-dry ice

With morpholine; hydrogenchloride; tert.-butyl lithium; copper(II) sulfate; magnesium; In tetrahydrofuran; 1,4-dioxane; ethanol; dichloromethane; pentane;