{4-[(4-{[(2Z)-2-(methoxyimino)-2-phenylethyl]oxy}benzyl)oxy]phenoxy}acetic acid

Base Information

Chemical Name:{4-[(4-{[(2Z)-2-(methoxyimino)-2-phenylethyl]oxy}benzyl)oxy]phenoxy}acetic acid
CAS No.:1356599-73-9
Molecular Formula:C₂₄H₂₃NO₆
Molecular Weight:421.45
Hs Code.:

Synonyms:{4-[(4-{[(2Z)-2-(methoxyimino)-2-phenylethyl]oxy}benzyl)oxy]phenoxy}acetic acid

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Chemical Property of {4-[(4-{[(2Z)-2-(methoxyimino)-2-phenylethyl]oxy}benzyl)oxy]phenoxy}acetic acid

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Technology Process of {4-[(4-{[(2Z)-2-(methoxyimino)-2-phenylethyl]oxy}benzyl)oxy]phenoxy}acetic acid

There total 6 articles about {4-[(4-{[(2Z)-2-(methoxyimino)-2-phenylethyl]oxy}benzyl)oxy]phenoxy}acetic 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: 49.5%

: 1356602-40-8
ethyl {4-[(4-{[(2Z)-2-(methoxyimino)-2-phenylethyl]oxy}benzyl)oxy]phenoxy}acetate

: 1356599-73-9
{4-[(4-{[(2Z)-2-(methoxyimino)-2-phenylethyl]oxy}benzyl)oxy]phenoxy}acetic acid

Guidance literature:: ethyl {4-[(4-{[(2Z)-2-(methoxyimino)-2-phenylethyl]oxy}benzyl)oxy]phenoxy}acetate; With water; sodium hydroxide; In tetrahydrofuran; ethanol; at 0 - 20 ℃; for 5h;

With hydrogenchloride; In diethyl ether; water; at 0 ℃;

Reference yield:

: 70-11-1
α-bromoacetophenone

: 1356599-73-9
{4-[(4-{[(2Z)-2-(methoxyimino)-2-phenylethyl]oxy}benzyl)oxy]phenoxy}acetic acid

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium acetate; acetic acid / 0.08 h / 20 °C

1.2: 3 h / 20 - 80 °C

2.1: potassium carbonate / acetonitrile / 0.08 h / 20 °C

2.2: 5 h / 20 - 80 °C

3.1: 1,1'-azodicarbonyl-dipiperidine; tributylphosphine / toluene / 3 h / 20 °C

4.1: sodium hydroxide; water / ethanol; tetrahydrofuran / 5 h / 0 - 20 °C

4.2: 0 °C

With tributylphosphine; water; sodium acetate; potassium carbonate; acetic acid; sodium hydroxide; 1,1'-azodicarbonyl-dipiperidine; In tetrahydrofuran; ethanol; toluene; acetonitrile;

Reference yield:

: 150-76-5
4-methoxy-phenol

: 1356599-73-9
{4-[(4-{[(2Z)-2-(methoxyimino)-2-phenylethyl]oxy}benzyl)oxy]phenoxy}acetic acid

Guidance literature:: Multi-step reaction with 4 steps

1.1: potassium carbonate / N,N-dimethyl-formamide / 5 h / 20 °C

2.1: boron tribromide / dichloromethane / 0 °C

2.2: 20 °C

3.1: 1,1'-azodicarbonyl-dipiperidine; tributylphosphine / toluene / 3 h / 20 °C

4.1: sodium hydroxide; water / ethanol; tetrahydrofuran / 5 h / 0 - 20 °C

4.2: 0 °C

With tributylphosphine; water; boron tribromide; potassium carbonate; sodium hydroxide; 1,1'-azodicarbonyl-dipiperidine; In tetrahydrofuran; ethanol; dichloromethane; N,N-dimethyl-formamide; toluene;