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HRID 257628作成日:2026年10月26日

2-Bromomethyl-4,5-diphenyl-oxazole → Methyl 3-[3-[(4,5-diphenyl-2-oxazolyl)-methoxy]phenyl]propanoate

https://huagongshe.com/reaction/257628

反応式

関与物質

役割名称HCID仕込み量
反応物2-Bromomethyl-4,5-diphenyl-oxazoleHCID 568599—
反応物Methyl 3-(3-hydroxyphenyl)propionateHCID 1512675—
生成物Methyl 3-[3-[(4,5-diphenyl-2-oxazolyl)-methoxy]phenyl]propanoateHCID 10070328833.6%

反応手順

A mixture of 2-bromomethyl-4,5-diphenyloxazole (10.00 g, 3 mmol), methyl 3-(3-hydroxyphenyl)propanoate (5.73 g, 3 mmol) potassium carbonate (4.83 g, 3.5 mmol) potassium iodide (catalytic amount) and acetonetrile (150 mL) was stirred at reflux temperature. After 30 minutes, the mixture was filtered, concentrated in vacuo and the residual oil chromatographed on a column of silica gel. Elution with a mixture of hexanes and diethyl ether (3:1) furnished methyl 3-[3-((4,5-diphenyl-2-oxazolyl)methoxy]phenyl]propanoate (10.34 g, 78%) as an oil. An analytical sample was prepared by subjecting a 4 g sample to chromatography under the conditions described above to furnish pure material as an oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05262540
出典データセットuspto-grants-1993_11
ORD IDord-e370f361ed2a458c9049b70c3aca86eb
出典メモuspto-grants-1993_11