3-{3-(2-Ethoxycarbonyl-ethyl)-4-[6-(4-fluoro-phenyl)-hexyloxy]-benzoyl}-benzoic acid ethyl ester

Base Information

Chemical Name:3-{3-(2-Ethoxycarbonyl-ethyl)-4-[6-(4-fluoro-phenyl)-hexyloxy]-benzoyl}-benzoic acid ethyl ester
CAS No.:117424-89-2
Molecular Formula:C₃₃H₃₇FO₆
Molecular Weight:548.652
Hs Code.:

Synonyms:3-{3-(2-Ethoxycarbonyl-ethyl)-4-[6-(4-fluoro-phenyl)-hexyloxy]-benzoyl}-benzoic acid ethyl ester

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Chemical Property of 3-{3-(2-Ethoxycarbonyl-ethyl)-4-[6-(4-fluoro-phenyl)-hexyloxy]-benzoyl}-benzoic acid ethyl ester

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Technology Process of 3-{3-(2-Ethoxycarbonyl-ethyl)-4-[6-(4-fluoro-phenyl)-hexyloxy]-benzoyl}-benzoic acid ethyl ester

There total 9 articles about 3-{3-(2-Ethoxycarbonyl-ethyl)-4-[6-(4-fluoro-phenyl)-hexyloxy]-benzoyl}-benzoic acid ethyl ester 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:

: 17814-85-6
(4-carboxybutyl)triphenylphosphonium bromide

: 117424-89-2
3-{3-(2-Ethoxycarbonyl-ethyl)-4-[6-(4-fluoro-phenyl)-hexyloxy]-benzoyl}-benzoic acid ethyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 1.) lithium hexamethyldisilazide / 1.) THF, hexane, 25 deg C, 1 h, 2.) 25 deg C, 2 h

2: 79 percent / H₂ / 5percent Pd/C / ethyl acetate / 1 h / 25 °C / 1551.4 Torr

3: 75 percent / LiAlH₄ / diethyl ether / 4 h / 25 °C

4: triethylamine (TEA) / diethyl ether

5: 1.) 60percent sodium hydride disp. in oil / 1.) DMF, 25 deg C, 30 min, 2.) 65 deg C

With lithium aluminium tetrahydride; hydrogen; sodium hydride; triethylamine; lithium hexamethyldisilazane; palladium on activated charcoal; In diethyl ether; ethyl acetate;
DOI:10.1021/jm00172a020

Reference yield:

: 459-57-4
4-fluorobenzaldehyde

: 117424-89-2
3-{3-(2-Ethoxycarbonyl-ethyl)-4-[6-(4-fluoro-phenyl)-hexyloxy]-benzoyl}-benzoic acid ethyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 1.) lithium hexamethyldisilazide / 1.) THF, hexane, 25 deg C, 1 h, 2.) 25 deg C, 2 h

2: 79 percent / H₂ / 5percent Pd/C / ethyl acetate / 1 h / 25 °C / 1551.4 Torr

3: 75 percent / LiAlH₄ / diethyl ether / 4 h / 25 °C

4: triethylamine (TEA) / diethyl ether

5: 1.) 60percent sodium hydride disp. in oil / 1.) DMF, 25 deg C, 30 min, 2.) 65 deg C

With lithium aluminium tetrahydride; hydrogen; sodium hydride; triethylamine; lithium hexamethyldisilazane; palladium on activated charcoal; In diethyl ether; ethyl acetate;
DOI:10.1021/jm00172a020

Reference yield:

: 128577-57-1
(E)-6-(4-fluorophenyl)hex-5-enoic acid

: 117424-89-2
3-{3-(2-Ethoxycarbonyl-ethyl)-4-[6-(4-fluoro-phenyl)-hexyloxy]-benzoyl}-benzoic acid ethyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 79 percent / H₂ / 5percent Pd/C / ethyl acetate / 1 h / 25 °C / 1551.4 Torr

2: 75 percent / LiAlH₄ / diethyl ether / 4 h / 25 °C

3: triethylamine (TEA) / diethyl ether

4: 1.) 60percent sodium hydride disp. in oil / 1.) DMF, 25 deg C, 30 min, 2.) 65 deg C

With lithium aluminium tetrahydride; hydrogen; sodium hydride; triethylamine; palladium on activated charcoal; In diethyl ether; ethyl acetate;
DOI:10.1021/jm00172a020