ethyl 1-(2-fluorobenzyl)-4-hydroxy-2-oxo-1,2-dihydroquinoline-3-carboxylate

Base Information

Chemical Name:ethyl 1-(2-fluorobenzyl)-4-hydroxy-2-oxo-1,2-dihydroquinoline-3-carboxylate
CAS No.:1415728-90-3
Molecular Formula:C₁₉H₁₆FNO₄
Molecular Weight:341.339
Hs Code.:

Synonyms:ethyl 1-(2-fluorobenzyl)-4-hydroxy-2-oxo-1,2-dihydroquinoline-3-carboxylate

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Chemical Property of ethyl 1-(2-fluorobenzyl)-4-hydroxy-2-oxo-1,2-dihydroquinoline-3-carboxylate

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Technology Process of ethyl 1-(2-fluorobenzyl)-4-hydroxy-2-oxo-1,2-dihydroquinoline-3-carboxylate

There total 3 articles about ethyl 1-(2-fluorobenzyl)-4-hydroxy-2-oxo-1,2-dihydroquinoline-3-carboxylate 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: 80.0%

: 57384-90-4
1-(2-fluorobenzyl)-1H-benzo[d][1,3]oxazine-2,4-dione

: 105-53-3
diethyl malonate

: 1415728-90-3
ethyl 1-(2-fluorobenzyl)-4-hydroxy-2-oxo-1,2-dihydroquinoline-3-carboxylate

Guidance literature:: diethyl malonate; With N,N-dimethyl acetamide; sodium hydride; In mineral oil; at 20 - 90 ℃;

1-(2-fluorobenzyl)-1H-benzo[d][1,3]oxazine-2,4-dione; In mineral oil; at 110 ℃;
DOI:10.1016/j.ejmech.2012.04.016

Reference yield:

: 118-48-9
isatoic anhydride

: 1415728-90-3
ethyl 1-(2-fluorobenzyl)-4-hydroxy-2-oxo-1,2-dihydroquinoline-3-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1.1: sodium hydride / N,N-dimethyl-formamide / 1 h / 20 °C

1.2: 18 h / 20 °C

2.1: N,N-dimethyl acetamide; sodium hydride / mineral oil / 20 - 90 °C

2.2: 110 °C

With N,N-dimethyl acetamide; sodium hydride; In N,N-dimethyl-formamide; mineral oil;
DOI:10.1016/j.ejmech.2012.04.016

Reference yield:

: 446-48-0
o-fluorobenzyl bromide

: 1415728-90-3
ethyl 1-(2-fluorobenzyl)-4-hydroxy-2-oxo-1,2-dihydroquinoline-3-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1.1: sodium hydride / N,N-dimethyl-formamide / 1 h / 20 °C

1.2: 18 h / 20 °C

2.1: N,N-dimethyl acetamide; sodium hydride / mineral oil / 20 - 90 °C

2.2: 110 °C

With N,N-dimethyl acetamide; sodium hydride; In N,N-dimethyl-formamide; mineral oil;
DOI:10.1016/j.ejmech.2012.04.016