4-(2-(allyloxy)-5-chlorophenyl)-3-(2-(tert-butyldiphenylsilyloxy)ethyl)-1-methyl-6-(trifluoromethyl)quinolin-2(1H)-one

Base Information

Chemical Name:4-(2-(allyloxy)-5-chlorophenyl)-3-(2-(tert-butyldiphenylsilyloxy)ethyl)-1-methyl-6-(trifluoromethyl)quinolin-2(1H)-one
CAS No.:930780-16-8
Molecular Formula:C₃₈H₃₇ClF₃NO₃Si
Molecular Weight:676.25
Hs Code.:

Synonyms:4-(2-(allyloxy)-5-chlorophenyl)-3-(2-(tert-butyldiphenylsilyloxy)ethyl)-1-methyl-6-(trifluoromethyl)quinolin-2(1H)-one

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Chemical Property of 4-(2-(allyloxy)-5-chlorophenyl)-3-(2-(tert-butyldiphenylsilyloxy)ethyl)-1-methyl-6-(trifluoromethyl)quinolin-2(1H)-one

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Technology Process of 4-(2-(allyloxy)-5-chlorophenyl)-3-(2-(tert-butyldiphenylsilyloxy)ethyl)-1-methyl-6-(trifluoromethyl)quinolin-2(1H)-one

There total 6 articles about 4-(2-(allyloxy)-5-chlorophenyl)-3-(2-(tert-butyldiphenylsilyloxy)ethyl)-1-methyl-6-(trifluoromethyl)quinolin-2(1H)-one 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:

: C₃₅H₃₃ClF₃NO₃Si

: 106-95-6
allyl bromide

: 930780-16-8
4-(2-(allyloxy)-5-chlorophenyl)-3-(2-(tert-butyldiphenylsilyloxy)ethyl)-1-methyl-6-(trifluoromethyl)quinolin-2(1H)-one

Guidance literature:: With potassium carbonate; In acetone; at 20 ℃; for 18h;
DOI:10.1021/jm061093j

Reference yield:

: 863225-72-3
3-[2-(tert-butyl-diphenyl-silanyloxy)-ethyl]-4-(5-chloro-2-hydroxy-phenyl)-6-trifluoromethyl-1H-quinolin-2-one

: 930780-16-8
4-(2-(allyloxy)-5-chlorophenyl)-3-(2-(tert-butyldiphenylsilyloxy)ethyl)-1-methyl-6-(trifluoromethyl)quinolin-2(1H)-one

Guidance literature:: Multi-step reaction with 4 steps

1: 6.82 g / Et₃N / CH₂Cl₂ / 4 h / 20 °C

2: 79 percent / K₂CO₃ / acetone / 18 h / 20 °C

3: LiOH*H₂O / ethanol / 4 h / 20 °C

4: 0.24 g / potassium carbonate / acetone / 18 h / 20 °C

With lithium hydroxide; potassium carbonate; triethylamine; In ethanol; dichloromethane; acetone;
DOI:10.1021/jm061093j

Reference yield:

: 721918-21-4
2-(3-(2-(tert-butyldiphenylsilyloxy)ethyl)-2-oxo-6-(trifluoromethyl)-1,2-dihydroquinolin-4-yl)-4-chlorophenyl acetate

: 930780-16-8
4-(2-(allyloxy)-5-chlorophenyl)-3-(2-(tert-butyldiphenylsilyloxy)ethyl)-1-methyl-6-(trifluoromethyl)quinolin-2(1H)-one

Guidance literature:: Multi-step reaction with 3 steps

1: 79 percent / K₂CO₃ / acetone / 18 h / 20 °C

2: LiOH*H₂O / ethanol / 4 h / 20 °C

3: 0.24 g / potassium carbonate / acetone / 18 h / 20 °C

With lithium hydroxide; potassium carbonate; In ethanol; acetone;
DOI:10.1021/jm061093j