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

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Chemical Name:ethyl 4-{4-[(4-{[(2E,2Z)-2-(methoxyimino)-2-phenylethyl]oxy}benzyl)oxy]phenyl}-5-methyl-1,2-oxazole-3-carboxylate
CAS No.:1356600-27-5
Molecular Formula:C₂₉H₂₈N₂O₆
Molecular Weight:500.551
Hs Code.:

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

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

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

There total 7 articles about ethyl 4-{4-[(4-{[(2E,2Z)-2-(methoxyimino)-2-phenylethyl]oxy}benzyl)oxy]phenyl}-5-methyl-1,2-oxazole-3-carboxylate 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: 54.0%

: 1356600-26-4
2-(4-(bromomethyl)phenoxy)-1-phenylethanone O-methyl oxime

: 1356600-25-3
ethyl 4-(4-hydroxyphenyl)-5-methyl-1,2-oxazole-3-carboxylate

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

Guidance literature:: With potassium carbonate; In acetonitrile; at 0 - 70 ℃; for 2h;

Reference yield:

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

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

Guidance literature:: Multi-step reaction with 3 steps

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

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

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

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

Reference yield:

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

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

Guidance literature:: Multi-step reaction with 4 steps

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

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

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

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

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