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

Base Information

Chemical Name:methyl 3-cyano-3-{2-methoxy-4-[(4-{[(2Z)-2-(methoxyimino)-2-phenylethyl]oxy}benzyl)oxy]phenyl}propanoate
CAS No.:1356600-87-7
Molecular Formula:C₂₈H₂₈N₂O₆
Molecular Weight:488.54
Hs Code.:

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

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

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

There total 9 articles about methyl 3-cyano-3-{2-methoxy-4-[(4-{[(2Z)-2-(methoxyimino)-2-phenylethyl]oxy}benzyl)oxy]phenyl}propanoate 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: 36.6%

: 1356600-84-4
methyl 3-cyano-3-(4-hydroxy-2-methoxyphenyl)propanoate

: 1356599-86-4
(4-{[(2Z)-2-(methoxyimino)-2-phenylethyl]oxy}phenyl)methanol

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

Guidance literature:: With tributylphosphine; 1,1'-azodicarbonyl-dipiperidine; In methanol; toluene; at 0 - 20 ℃; for 4h;

Reference yield:

: 52085-14-0
4-benzoxy-salicylaldehyde

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

Guidance literature:: Multi-step reaction with 6 steps

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

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

3: methanol / 2 h / 70 °C

4: methanesulfonic acid / 2 h / 65 °C

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

6: 1,1'-azodicarbonyl-dipiperidine; tributylphosphine / toluene; methanol / 4 h / 0 - 20 °C

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

Reference yield:

: 95-01-2
2,4-Dihydroxybenzaldehyde

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

Guidance literature:: Multi-step reaction with 7 steps

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

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

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

4: methanol / 2 h / 70 °C

5: methanesulfonic acid / 2 h / 65 °C

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

7: 1,1'-azodicarbonyl-dipiperidine; tributylphosphine / toluene; methanol / 4 h / 0 - 20 °C

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