4-{4-[(4-{[(2E,2Z)-2-(methoxyimino)-2-phenylethyl]oxy}benzyl)oxy]phenyl}-5-methyl-1,2-oxazole-3-carboxylic acid

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Chemical Name:4-{4-[(4-{[(2E,2Z)-2-(methoxyimino)-2-phenylethyl]oxy}benzyl)oxy]phenyl}-5-methyl-1,2-oxazole-3-carboxylic acid
CAS No.:1356598-88-3
Molecular Formula:C₂₇H₂₄N₂O₆
Molecular Weight:472.497
Hs Code.:

Synonyms:4-{4-[(4-{[(2E,2Z)-2-(methoxyimino)-2-phenylethyl]oxy}benzyl)oxy]phenyl}-5-methyl-1,2-oxazole-3-carboxylic acid

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Chemical Property of 4-{4-[(4-{[(2E,2Z)-2-(methoxyimino)-2-phenylethyl]oxy}benzyl)oxy]phenyl}-5-methyl-1,2-oxazole-3-carboxylic acid

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Technology Process of 4-{4-[(4-{[(2E,2Z)-2-(methoxyimino)-2-phenylethyl]oxy}benzyl)oxy]phenyl}-5-methyl-1,2-oxazole-3-carboxylic acid

There total 8 articles about 4-{4-[(4-{[(2E,2Z)-2-(methoxyimino)-2-phenylethyl]oxy}benzyl)oxy]phenyl}-5-methyl-1,2-oxazole-3-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: 38.8%

: 1356600-27-5
ethyl 4-{4-[(4-{[(2E,2Z)-2-(methoxyimino)-2-phenylethyl]oxy}benzyl)oxy]phenyl}-5-methyl-1,2-oxazole-3-carboxylate

: 1356598-88-3
4-{4-[(4-{[(2E,2Z)-2-(methoxyimino)-2-phenylethyl]oxy}benzyl)oxy]phenyl}-5-methyl-1,2-oxazole-3-carboxylic acid

Guidance literature:: ethyl 4-{4-[(4-{[(2E,2Z)-2-(methoxyimino)-2-phenylethyl]oxy}benzyl)oxy]phenyl}-5-methyl-1,2-oxazole-3-carboxylate; With water; sodium hydroxide; In tetrahydrofuran; ethanol; at 20 ℃;

With hydrogenchloride; In water; at 20 ℃; pH=2;

Reference yield:

: 3209-72-1
ethyl 5-methylisoxazole-3-carboxylate

: 1356598-88-3
4-{4-[(4-{[(2E,2Z)-2-(methoxyimino)-2-phenylethyl]oxy}benzyl)oxy]phenyl}-5-methyl-1,2-oxazole-3-carboxylic acid

Guidance literature:: Multi-step reaction with 4 steps

1.1: trifluoroacetic acid; N-iodo-succinimide / 3 h / 65 °C

2.1: sodium hydrogencarbonate / bis-triphenylphosphine-palladium(II) chloride / N,N-dimethyl-formamide / 5 h / 95 °C / Inert atmosphere

3.1: potassium carbonate / acetonitrile / 2 h / 0 - 70 °C

4.1: sodium hydroxide; water / ethanol; tetrahydrofuran / 20 °C

4.2: 20 °C / pH 2

With N-iodo-succinimide; water; sodium hydrogencarbonate; potassium carbonate; trifluoroacetic acid; sodium hydroxide; bis-triphenylphosphine-palladium(II) chloride; In tetrahydrofuran; ethanol; N,N-dimethyl-formamide; acetonitrile;

Reference yield:

: 615-79-2
ethyl 2,4-diketopentanoate

: 1356598-88-3
4-{4-[(4-{[(2E,2Z)-2-(methoxyimino)-2-phenylethyl]oxy}benzyl)oxy]phenyl}-5-methyl-1,2-oxazole-3-carboxylic acid

Guidance literature:: Multi-step reaction with 5 steps

1.1: hydroxylamine hydrochloride; sodium hydrogencarbonate / ethanol / 8 h / 80 °C / Inert atmosphere

2.1: trifluoroacetic acid; N-iodo-succinimide / 3 h / 65 °C

3.1: sodium hydrogencarbonate / bis-triphenylphosphine-palladium(II) chloride / N,N-dimethyl-formamide / 5 h / 95 °C / Inert atmosphere

4.1: potassium carbonate / acetonitrile / 2 h / 0 - 70 °C

5.1: sodium hydroxide; water / ethanol; tetrahydrofuran / 20 °C

5.2: 20 °C / pH 2

With N-iodo-succinimide; hydroxylamine hydrochloride; water; sodium hydrogencarbonate; potassium carbonate; trifluoroacetic acid; sodium hydroxide; bis-triphenylphosphine-palladium(II) chloride; In tetrahydrofuran; ethanol; N,N-dimethyl-formamide; acetonitrile;