7-(4-(4-chlorobenzyloxycarbamoyl)phenoxy)-6-cyanochroman-4-carboxylic acid

Base Information

Chemical Name:7-(4-(4-chlorobenzyloxycarbamoyl)phenoxy)-6-cyanochroman-4-carboxylic acid
CAS No.:1202886-89-2
Molecular Formula:C₂₅H₁₉ClN₂O₆
Molecular Weight:478.889
Hs Code.:

Synonyms:7-(4-(4-chlorobenzyloxycarbamoyl)phenoxy)-6-cyanochroman-4-carboxylic acid

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Chemical Property of 7-(4-(4-chlorobenzyloxycarbamoyl)phenoxy)-6-cyanochroman-4-carboxylic acid

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Technology Process of 7-(4-(4-chlorobenzyloxycarbamoyl)phenoxy)-6-cyanochroman-4-carboxylic acid

There total 9 articles about 7-(4-(4-chlorobenzyloxycarbamoyl)phenoxy)-6-cyanochroman-4-carboxylic acid 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: 82.3%

: 1202889-88-0
methyl 7-(4-((4-chlorobenzyloxy)carbamoyl)phenoxy)-6-cyano-3,4-dihydro-2H-chromene-4-carboxylate

: 1202886-89-2
7-(4-(4-chlorobenzyloxycarbamoyl)phenoxy)-6-cyanochroman-4-carboxylic acid

Guidance literature:: methyl 7-(4-((4-chlorobenzyloxy)carbamoyl)phenoxy)-6-cyano-3,4-dihydro-2H-chromene-4-carboxylate; With water; sodium hydroxide; In tetrahydrofuran; methanol; for 2h;

With hydrogenchloride; In tetrahydrofuran; methanol; water; ethyl acetate;

Reference yield:

: 1202889-76-6
methyl 6-cyano-7-fluorochroman-4-carboxylate

: 1202886-89-2
7-(4-(4-chlorobenzyloxycarbamoyl)phenoxy)-6-cyanochroman-4-carboxylic acid

Guidance literature:: Multi-step reaction with 4 steps

1.1: potassium carbonate / 1-methyl-pyrrolidin-2-one / 18 h / 115 °C / Molecular sieve; Inert atmosphere

2.1: trifluoroacetic acid / dichloromethane / 1.5 h / 20 °C

3.1: oxalyl dichloride; N,N-dimethyl-formamide / dichloromethane / 0.33 h

3.2: 0.5 h

4.1: water; sodium hydroxide / tetrahydrofuran; methanol / 2 h

With oxalyl dichloride; water; potassium carbonate; N,N-dimethyl-formamide; trifluoroacetic acid; sodium hydroxide; In tetrahydrofuran; 1-methyl-pyrrolidin-2-one; methanol; dichloromethane;

Reference yield:

: 113209-68-0
3,4-dihydro-7-fluoro-2H-1-benzopyran-4-one

: 1202886-89-2
7-(4-(4-chlorobenzyloxycarbamoyl)phenoxy)-6-cyanochroman-4-carboxylic acid

Guidance literature:: Multi-step reaction with 9 steps

1.1: zinc(II) iodide / 4 h / 20 °C

2.1: hydrogenchloride; tin(II) chloride dihdyrate / water; acetic acid / 130 °C

3.1: sulfuric acid / tetrahydrofuran / 12 h / 55 °C

4.1: N-Bromosuccinimide / N,N-dimethyl-formamide / 2.5 h / 50 °C

5.1: 1-methyl-pyrrolidin-2-one / 6 h / 160 °C / Inert atmosphere

6.1: potassium carbonate / 1-methyl-pyrrolidin-2-one / 18 h / 115 °C / Molecular sieve; Inert atmosphere

7.1: trifluoroacetic acid / dichloromethane / 1.5 h / 20 °C

8.1: oxalyl dichloride; N,N-dimethyl-formamide / dichloromethane / 0.33 h

8.2: 0.5 h

9.1: water; sodium hydroxide / tetrahydrofuran; methanol / 2 h

With hydrogenchloride; N-Bromosuccinimide; oxalyl dichloride; tin(II) chloride dihdyrate; sulfuric acid; water; potassium carbonate; N,N-dimethyl-formamide; trifluoroacetic acid; sodium hydroxide; zinc(II) iodide; In tetrahydrofuran; 1-methyl-pyrrolidin-2-one; methanol; dichloromethane; water; acetic acid; N,N-dimethyl-formamide;