3-cyano-3-{2-methoxy-4-[(4-{[(2Z)-2-(methoxyimino)-2-phenylethyl]oxy}benzyl)oxy]phenyl}propanoic acid

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Chemical Name:3-cyano-3-{2-methoxy-4-[(4-{[(2Z)-2-(methoxyimino)-2-phenylethyl]oxy}benzyl)oxy]phenyl}propanoic acid
CAS No.:1356599-39-7
Molecular Formula:C₂₇H₂₆N₂O₆
Molecular Weight:474.513
Hs Code.:

Synonyms:3-cyano-3-{2-methoxy-4-[(4-{[(2Z)-2-(methoxyimino)-2-phenylethyl]oxy}benzyl)oxy]phenyl}propanoic acid

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Chemical Property of 3-cyano-3-{2-methoxy-4-[(4-{[(2Z)-2-(methoxyimino)-2-phenylethyl]oxy}benzyl)oxy]phenyl}propanoic acid

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Technology Process of 3-cyano-3-{2-methoxy-4-[(4-{[(2Z)-2-(methoxyimino)-2-phenylethyl]oxy}benzyl)oxy]phenyl}propanoic acid

There total 10 articles about 3-cyano-3-{2-methoxy-4-[(4-{[(2Z)-2-(methoxyimino)-2-phenylethyl]oxy}benzyl)oxy]phenyl}propanoic 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: 6.86%

: 1356600-87-7
methyl 3-cyano-3-{2-methoxy-4-[(4-{[(2Z)-2-(methoxyimino)-2-phenylethyl]oxy}benzyl)oxy]phenyl}propanoate

: 1356599-39-7
3-cyano-3-{2-methoxy-4-[(4-{[(2Z)-2-(methoxyimino)-2-phenylethyl]oxy}benzyl)oxy]phenyl}propanoic acid

Guidance literature:: methyl 3-cyano-3-{2-methoxy-4-[(4-{[(2Z)-2-(methoxyimino)-2-phenylethyl]oxy}benzyl)oxy]phenyl}propanoate; With water; sodium hydroxide; In tetrahydrofuran; methanol; at 0 ℃; for 30h;

With citric acid; In water; at 20 ℃; pH=6;

Reference yield:

: 52085-14-0
4-benzoxy-salicylaldehyde

: 1356599-39-7
3-cyano-3-{2-methoxy-4-[(4-{[(2Z)-2-(methoxyimino)-2-phenylethyl]oxy}benzyl)oxy]phenyl}propanoic acid

Guidance literature:: Multi-step reaction with 7 steps

1.1: potassium carbonate / acetonitrile / 16 h / 0 - 20 °C

2.1: piperidine; acetic acid / toluene / 5 h / 125 °C

3.1: methanol / 2 h / 70 °C

4.1: methanesulfonic acid / 2 h / 65 °C

5.1: hydrogen / palladium 10% on activated carbon / ethyl acetate / 1 h / 20 °C

6.1: 1,1'-azodicarbonyl-dipiperidine; tributylphosphine / toluene; methanol / 4 h / 0 - 20 °C

7.1: sodium hydroxide; water / tetrahydrofuran; methanol / 30 h / 0 °C

7.2: 20 °C / pH 6

With piperidine; methanesulfonic acid; tributylphosphine; water; hydrogen; potassium carbonate; acetic acid; sodium hydroxide; 1,1'-azodicarbonyl-dipiperidine; palladium 10% on activated carbon; In tetrahydrofuran; methanol; ethyl acetate; toluene; acetonitrile;

Reference yield:

: 95-01-2
2,4-Dihydroxybenzaldehyde

: 1356599-39-7
3-cyano-3-{2-methoxy-4-[(4-{[(2Z)-2-(methoxyimino)-2-phenylethyl]oxy}benzyl)oxy]phenyl}propanoic acid

Guidance literature:: Multi-step reaction with 8 steps

1.1: potassium carbonate / acetonitrile / 3 h / 20 °C

2.1: potassium carbonate / acetonitrile / 16 h / 0 - 20 °C

3.1: piperidine; acetic acid / toluene / 5 h / 125 °C

4.1: methanol / 2 h / 70 °C

5.1: methanesulfonic acid / 2 h / 65 °C

6.1: hydrogen / palladium 10% on activated carbon / ethyl acetate / 1 h / 20 °C

7.1: 1,1'-azodicarbonyl-dipiperidine; tributylphosphine / toluene; methanol / 4 h / 0 - 20 °C

8.1: sodium hydroxide; water / tetrahydrofuran; methanol / 30 h / 0 °C

8.2: 20 °C / pH 6

With piperidine; methanesulfonic acid; tributylphosphine; water; hydrogen; potassium carbonate; acetic acid; sodium hydroxide; 1,1'-azodicarbonyl-dipiperidine; palladium 10% on activated carbon; In tetrahydrofuran; methanol; ethyl acetate; toluene; acetonitrile;