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

Base Information

Chemical Name:acetic acid 3-cyclohex-2-enyl-1-methyl-2-oxo-1,2-dihydro-quinolin-4-yl ester
CAS No.:211686-46-3
Molecular Formula:C₁₈H₁₉NO₃
Molecular Weight:297.354
Hs Code.:

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

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Chemical Property of acetic acid 3-cyclohex-2-enyl-1-methyl-2-oxo-1,2-dihydro-quinolin-4-yl ester

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Technology Process of acetic acid 3-cyclohex-2-enyl-1-methyl-2-oxo-1,2-dihydro-quinolin-4-yl ester

There total 4 articles about acetic acid 3-cyclohex-2-enyl-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: 95.0%

: 127-09-3
sodium acetate

: 211686-40-7
3-cyclohex-2-enyl-4-hydroxy-1-methylquinolin-2(1H)-one

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

Guidance literature:: In acetic anhydride; for 3h; Heating;
DOI:10.1080/00397919808004868

Reference yield:

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

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

Guidance literature:: Multi-step reaction with 2 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

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

Reference yield:

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

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

Guidance literature:: Multi-step reaction with 3 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

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