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

Base Information

Chemical Name:({4-[(4-{[(2E,2Z)-2-(methoxyimino)-2-phenylethyl]oxy}benzyl)oxy]benzyl}oxy)acetic acid
CAS No.:1356598-86-1
Molecular Formula:C₂₅H₂₅NO₆
Molecular Weight:435.477
Hs Code.:

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

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

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

There total 5 articles about ({4-[(4-{[(2E,2Z)-2-(methoxyimino)-2-phenylethyl]oxy}benzyl)oxy]benzyl}oxy)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: 6.25%

: 1356600-23-1
{4-[(4-{[(2E,2Z)-2-(methoxyimino)-2-phenylethyl]oxy}benzyl)oxy]phenyl}methanol

: 79-08-3
bromoacetic acid

: 1356598-86-1
({4-[(4-{[(2E,2Z)-2-(methoxyimino)-2-phenylethyl]oxy}benzyl)oxy]benzyl}oxy)acetic acid

Guidance literature:: With sodium hydride; In tetrahydrofuran; at 0 - 20 ℃; for 13h;

Reference yield:

: 70-11-1
α-bromoacetophenone

: 1356598-86-1
({4-[(4-{[(2E,2Z)-2-(methoxyimino)-2-phenylethyl]oxy}benzyl)oxy]benzyl}oxy)acetic acid

Guidance literature:: Multi-step reaction with 5 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: triphenylphosphine; di-isopropyl azodicarboxylate / tetrahydrofuran / 16 h / 0 - 20 °C

4.1: sodium tetrahydroborate; methanol / 1.25 h / 0 - 20 °C

5.1: sodium hydride / tetrahydrofuran / 13 h / 0 - 20 °C

With methanol; sodium tetrahydroborate; di-isopropyl azodicarboxylate; sodium acetate; sodium hydride; potassium carbonate; acetic acid; triphenylphosphine; In tetrahydrofuran; acetonitrile;

Reference yield:

: 1356600-22-0
4-[(4-{[(2E,2Z)-2-(methoxyimino)-2-phenylethyl]oxy}benzyl)oxy]benzaldehyde

: 1356598-86-1
({4-[(4-{[(2E,2Z)-2-(methoxyimino)-2-phenylethyl]oxy}benzyl)oxy]benzyl}oxy)acetic acid

Guidance literature:: Multi-step reaction with 2 steps

1: sodium tetrahydroborate; methanol / 1.25 h / 0 - 20 °C

2: sodium hydride / tetrahydrofuran / 13 h / 0 - 20 °C

With methanol; sodium tetrahydroborate; sodium hydride; In tetrahydrofuran;