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HRID 335392作成日:2026年10月25日

Potassium Hydroxide → 7-[4-Nitro-3-(trifluoromethyl)phenyl]-7-azabicyclo[2.2.1]heptane

https://huagongshe.com/reaction/335392

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium HydroxideHCID 14797—
反応物5-Fluoro-2-nitrobenzotrifluorideHCID 223094—
反応物7-Azabicyclo[2.2.1]heptane hydrochlorideHCID 16279503—
触媒Tetrabutylammonium BromideHCID 74236—
溶媒DichloromethaneHCID 6344—
生成物7-[4-Nitro-3-(trifluoromethyl)phenyl]-7-azabicyclo[2.2.1]heptaneHCID 57516843—

反応手順

4-fluoro-1-nitro-2-(trifluoromethyl)benzene was dissolved in 3 vol DCM. Tetrabutylammoniumbromide (0.05 eq) and KOH (50 wt %, 3.6 eq) were added. 7-azabicyclo[2.2.1]heptane hydrochloride (8-HCl) was then added at 0-5° C. The reaction was warmed up to ambient temperature and monitored by HPLC. Once substantially complete, the layers were separated and the organic layer was washed with 1M HCl. The layers were separated and the aqueous layer was discarded. The organic layer was washed once with water, once with brine, and then distilled. The resulting material was recrystallized from cyclohexane at reflux. The solid was filtered, washed with cyclohexane, and dried in a vacuum oven at 45° C. with a N2 gas bleed to provide 7-[4-nitro-3-(trifluoromethyl)phenyl]-7-azabicyclo[2.2.1]heptane (9).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08884018B2
出典データセットuspto-grants-2014_11
ORD IDord-15aba32715384f66828f7e2d969d7239
出典メモuspto-grants-2014_11