acetic acid 3-(2,3-dibromo-cyclohexyl)-1-methyl-2-oxo-1,2-dihydro-quinolin-4-yl ester

Base Information

Chemical Name:acetic acid 3-(2,3-dibromo-cyclohexyl)-1-methyl-2-oxo-1,2-dihydro-quinolin-4-yl ester
CAS No.:211686-47-4
Molecular Formula:C₁₈H₁₉Br₂NO₃
Molecular Weight:457.162
Hs Code.:

Synonyms:acetic acid 3-(2,3-dibromo-cyclohexyl)-1-methyl-2-oxo-1,2-dihydro-quinolin-4-yl ester

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Chemical Property of acetic acid 3-(2,3-dibromo-cyclohexyl)-1-methyl-2-oxo-1,2-dihydro-quinolin-4-yl ester

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Technology Process of acetic acid 3-(2,3-dibromo-cyclohexyl)-1-methyl-2-oxo-1,2-dihydro-quinolin-4-yl ester

There total 5 articles about acetic acid 3-(2,3-dibromo-cyclohexyl)-1-methyl-2-oxo-1,2-dihydro-quinolin-4-yl 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: 90.0%

: 211686-46-3
acetic acid 3-cyclohex-2-enyl-1-methyl-2-oxo-1,2-dihydro-quinolin-4-yl ester

: 211686-47-4
acetic acid 3-(2,3-dibromo-cyclohexyl)-1-methyl-2-oxo-1,2-dihydro-quinolin-4-yl ester

Guidance literature:: With bromine; In acetic acid; at 20 ℃; for 2h;
DOI:10.1080/00397919808004868

Reference yield:

: 1521-51-3,113667-32-6
rac-3-bromocyclohexene

: 211686-47-4
acetic acid 3-(2,3-dibromo-cyclohexyl)-1-methyl-2-oxo-1,2-dihydro-quinolin-4-yl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 40 percent / 30 percent aq. NaOH / tetrabutylammoniumbromide (TBAB) / CH₂Cl₂ / 1 h / 20 °C / phase transfer catalyse

2: 95 percent / acetic anhydride / 3 h / Heating

3: 90 percent / Br₂ / acetic acid / 2 h / 20 °C

With sodium hydroxide; bromine; tetrabutylammomium bromide; In dichloromethane; acetic anhydride; acetic acid; 1: Alkylation / 2: Acetylation / 3: Bromination;
DOI:10.1080/00397919808004868

Reference yield:

: 1677-46-9
4-hydroxy-1-methyl-2(1H)-quinolone

: 211686-47-4
acetic acid 3-(2,3-dibromo-cyclohexyl)-1-methyl-2-oxo-1,2-dihydro-quinolin-4-yl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 20 percent / 30 percent aq. NaOH / tetrabutylammoniumbromide (TBAB) / CH₂Cl₂ / 1 h / 20 °C / phase transfer catalyse

2: 90 percent / chlorobenzene / Heating

3: 95 percent / acetic anhydride / 3 h / Heating

4: 90 percent / Br₂ / acetic acid / 2 h / 20 °C

With sodium hydroxide; bromine; tetrabutylammomium bromide; In dichloromethane; acetic anhydride; acetic acid; chlorobenzene; 1: Alkylation / 2: Rearrangement / 3: Acetylation / 4: Bromination;
DOI:10.1080/00397919808004868