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HRID 436684作成日:2026年10月26日

Ammonium Hydroxide → 4-[(3,6-Dichloropyridin-2-yl)methoxy]aniline

https://huagongshe.com/reaction/436684

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium HydroxideHCID 14923—
反応物N-{4-[(3,6-Dichloropyridin-2-yl)methoxy]phenyl}acetamideHCID 20366210—
溶媒Boron, trifluoro(methanol)-, (T-4)-HCID 11062313—
生成物4-[(3,6-Dichloropyridin-2-yl)methoxy]anilineHCID 20366173—

反応手順

N-(4-((3,6-Dichloro-2-pyridinyl)methoxy)phenyl)acetamide (30.27 grams; 0.097 mole) was mixed with a 270 ml. solution of boron trifluoride-methanol (1 gram per 10 ml.) and the resulting reaction mixture refluxed for a period of 41/2 hours. The reaction mixture was then diluted and cooled with ice water to a temperature of between about 0° to about 10° C. Concentrated ammonium hydroxide was added until the reaction mixture was basic. The reaction mixture was then extracted with portions of methylene chloride, the extracts combined and the solvent removed by evaporation. The residue thus obtained was extracted with five 500 ml. portions of hexane. The crystalline material which precipitated from the hexane mixture upon cooling was recovered by filtration. As a result of these operations, the desired 4-((3,6-dichloro-2-pyridinyl)methoxy)benzenamine compound was recovered as a light yellow crystalline solid having a melting point of 74° -75° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04028092
出典データセットuspto-grants-1977_06
ORD IDord-ee71a9a5c11d4e93befd2835cd7c9de2
出典メモuspto-grants-1977_06