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HRID 233837作成日:2026年10月25日

Acetonitrile → 6-Fluoro-3-[1-(3-phenoxypropyl)-4-piperidinyl]1,2-benzisoxazole

https://huagongshe.com/reaction/233837

反応式

関与物質

役割名称HCID仕込み量
反応物AcetonitrileHCID 6342—
反応物Potassium CarbonateHCID 11430—
反応物(3-Chloropropoxy)benzeneHCID 76917—
反応物3-(4-Piperidyl)-6-fluoro-1,2-benzisoxazoleHCID 849421—
溶媒WaterHCID 962—
生成物6-Fluoro-3-[1-(3-phenoxypropyl)-4-piperidinyl]1,2-benzisoxazoleHCID 1047332047%

反応手順

A mixture of 6-fluoro-3-(4-piperidinyl)-1,2-benzisoxazole (4.0 g, 18.2 mmol), K2CO3 (3.0 g, 21.8 mmol), KI (100 mg), 3-chloropropoxybenzene (3.4 g, 20.0 mmol), and acetonitrile was stirred at reflux under nitrogen for 30 hours. The reaction was poured into water and the aqueous mixture was extracted with ethyl acetate. The ethyl acetate extract was washed with brine, dried with MgSO4 and concentrated to afford 6.2 g of a damp, beige solid. The compound was recrystallized twice from ethanol to yield (47%) of 6-fluoro-3-[1-(3-phenoxypropyl)-4-piperidinyl]-1,2-benzisoxazole as a light beige solid, m.p.=78°-80° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05593995
出典データセットuspto-grants-1997_01
ORD IDord-ee84f73ec37f41e9b6928389914e9576
出典メモuspto-grants-1997_01