(1R,4R)-4-(tert-butyldiphenylsilyloxy)-7-fluoro-1,2,3,4-tetrahydronaphthalen-1-amine

Base Information

Chemical Name:(1R,4R)-4-(tert-butyldiphenylsilyloxy)-7-fluoro-1,2,3,4-tetrahydronaphthalen-1-amine
CAS No.:1083302-43-5
Molecular Formula:C₂₆H₃₀FNOSi
Molecular Weight:419.614
Hs Code.:

Synonyms:(1R,4R)-4-(tert-butyldiphenylsilyloxy)-7-fluoro-1,2,3,4-tetrahydronaphthalen-1-amine

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Chemical Property of (1R,4R)-4-(tert-butyldiphenylsilyloxy)-7-fluoro-1,2,3,4-tetrahydronaphthalen-1-amine

Chemical Property:

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Technology Process of (1R,4R)-4-(tert-butyldiphenylsilyloxy)-7-fluoro-1,2,3,4-tetrahydronaphthalen-1-amine

There total 8 articles about (1R,4R)-4-(tert-butyldiphenylsilyloxy)-7-fluoro-1,2,3,4-tetrahydronaphthalen-1-amine 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:

: 1083302-41-3
N-((1R,4R)-4-(tert-butyldiphenylsilyloxy)-7-fluoro-1,2,3,4-tetrahydronaphthalen-1-yl)-2,2,2-trifluoroacetamide

: 1083302-43-5
(1R,4R)-4-(tert-butyldiphenylsilyloxy)-7-fluoro-1,2,3,4-tetrahydronaphthalen-1-amine

Guidance literature:: With potassium carbonate; In methanol; water; at 50 ℃; for 72h;

Reference yield:

: 1083302-30-0
(S)-7-fluoro-1-tetralol

: 1083302-43-5
(1R,4R)-4-(tert-butyldiphenylsilyloxy)-7-fluoro-1,2,3,4-tetrahydronaphthalen-1-amine

Guidance literature:: Multi-step reaction with 7 steps

1.1: 1,8-diazabicyclo[5.4.0]undec-7-ene / toluene

1.2: 0 - 20 °C

2.1: hydrogen / palladium 10% on activated carbon / methanol / 1810.07 Torr

3.1: triethylamine; trifluoroacetic anhydride / dichloromethane / 16.33 h / 0 - 20 °C

4.1: potassium permanganate; magnesium sulfate / water; acetone / 17 h / 0 - 20 °C

5.1: formic acid; triethylamine / Noyori's catalyst / N,N-dimethyl-formamide / 0 - 40 °C

6.1: 1H-imidazole / N,N-dimethyl-formamide / 16 h / 0 - 20 °C

7.1: potassium carbonate / methanol; water / 72 h / 50 °C

With 1H-imidazole; potassium permanganate; formic acid; hydrogen; magnesium sulfate; potassium carbonate; 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; trifluoroacetic anhydride; Noyori's catalyst; palladium 10% on activated carbon; In methanol; dichloromethane; water; N,N-dimethyl-formamide; acetone; toluene;

Reference yield:

: 1083302-35-5
(R)-2,2,2-trifluoro-N-(7-fluoro-1,2,3,4-tetrahydronaphthalen-1-yl)acetamide

: 1083302-43-5
(1R,4R)-4-(tert-butyldiphenylsilyloxy)-7-fluoro-1,2,3,4-tetrahydronaphthalen-1-amine

Guidance literature:: Multi-step reaction with 4 steps

1: potassium permanganate; magnesium sulfate / water; acetone / 17 h / 0 - 20 °C

2: formic acid; triethylamine / Noyori's catalyst / N,N-dimethyl-formamide / 0 - 40 °C

3: 1H-imidazole / N,N-dimethyl-formamide / 16 h / 0 - 20 °C

4: potassium carbonate / methanol; water / 72 h / 50 °C

With 1H-imidazole; potassium permanganate; formic acid; magnesium sulfate; potassium carbonate; triethylamine; Noyori's catalyst; In methanol; water; N,N-dimethyl-formamide; acetone;