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HRID 404619作成日:2026年10月26日

Benzoyl chloride → 3-(Chloromethyl)-5-phenyl-1,2,4-oxadiazole

https://huagongshe.com/reaction/404619

反応式

関与物質

役割名称HCID仕込み量
反応物Benzoyl chlorideHCID 7412—
反応物2-chloro-N'-hydroxyethanimidamideHCID 4112252—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物3-(Chloromethyl)-5-phenyl-1,2,4-oxadiazoleHCID 30215444.8%

反応手順

Benzoyl chloride (1.60 ml, 13.8 mmol) was added to a suspension of 2-chloro-N′-hydroxyacetimidamide (1.0 g, 9.21 mmol) in DCM (25 ml), with stirring at room temperature. After 30 minutes, TEA (1.41 ml, 10.1 mmol) was added to the white suspension and the mixture was stirred for 30 additional minutes (UPLC-MS: complete conversion). The solution was diluted with DCM (20 ml) and water (30 ml) was added. The aqueous phase was extracted three times with DCM (15 ml×3) and then the combined organic phases were dried (Na2SO4) and evaporated. The crude was suspended in toluene (25 ml) and the mixture was heated to reflux for 6 h (UPLC-MS: complete conversion). The solvent was evaporated and the crude was purified by flash chromatography (petroleum ether/EtOAc=95/5) to obtain 3-(chloromethyl)-5-phenyl-1,2,4-oxadiazole (803 mg, 44.8% yield) as an off-white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08748613B2
出典データセットuspto-grants-2014_06
ORD IDord-031cd1f1b49c48b4b287179e59899b42
出典メモuspto-grants-2014_06