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HRID 2088134作成日:2026年10月25日

Benzyl Bromide → (1R*,2R*,5R*)-8-Benzyl-2-[2,5-bis(trifluoromethyl)phenylmethoxy]-1-phenyl-8-azabicyclo[3.2.1]octane

https://huagongshe.com/reaction/2088134

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl BromideHCID 7498—
反応物Sodium hydrideHCID 24758—
反応物2-(Bromomethyl)-1,4-bis(trifluoromethyl)benzeneHCID 2773199—
反応物(1R*,2R*,5R*)-8-Benzyl-1-phenyl-8-azabicyclo[3.2.1]octan-2-olHCID 69688994—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物(1R*,2R*,5R*)-8-Benzyl-2-[2,5-bis(trifluoromethyl)phenylmethoxy]-1-phenyl-8-azabicyclo[3.2.1]octaneHCID 86586657—

反応手順

(1R*,2R*,5R*)-8-Benzyl-1-phenyl-8-azabicyclo[3.2.1]octan-2-ol (Description 9; 151 mg, 0.52 mmol) was treated with sodium hydride (41 mg, 60% in oil, 1.03 mmol) at 0° C. in a solution of THF (2 ml) and allowed to warm to room temperature. The mixture was recooled to 0° C. and 2,5-bis(trifluoromethyl)benzyl bromide (0.24 ml, 1.30 mmol) added and the mixture heated to 50° C. for 2 days. A further 1.30 mmol of the benzyl bromide was added and the mixture further heated for 50° C. for 2 days. The reaction mixture was poured into water and extracted with ethyl acetate (×3), dried (MgSO4) and concentrated in vacuo to give a yellow solid. This was purified by flash column chromatography [25% ethyl acetate in iso-hexane] to give the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06727249B2
出典データセットuspto-grants-2004_04
ORD IDord-3985ac8dd7a14528a1ab2784fd7fa7cb
出典メモuspto-grants-2004_04