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HRID 533385作成日:2026年10月26日

Ethanol → (S)-3-[(R)-2-Ethoxy-1-(naphthalen-1-yloxy)ethyl]pyrrolidine

https://huagongshe.com/reaction/533385

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物1-FluoronaphthaleneHCID 9450—
反応物Sodium hydrideHCID 24758—
反応物(S)-3-((R)-2-Ethoxy-1-hydroxyethyl)pyrrolidine-1-carboxylic Acid t-Butyl EsterHCID 66858889—
溶媒Hydrochloric AcidHCID 313—
溶媒DimethylformamideHCID 6228—
生成物(S)-3-[(R)-2-Ethoxy-1-(naphthalen-1-yloxy)ethyl]pyrrolidineHCID 58120253—

反応手順

(S)-3-((R)-2-Ethoxy-1-hydroxyethyl)pyrrolidine-1-carboxylic acid t-butyl ester (200 mg, 0.8 mmol) and 1-fluoronaphthalene were dissolved in DMF (2.7 mL). NaH (27.8 mg, 1.2 mmol) was added and the mixture was stirred at room temperature for 15 minutes, then heated at 120° C. for 4 hours. The mixture was then cooled to room temperature. The mixture was concentrated then dissolved in 1.2M HCl in EtOH (19 mL, 23 mmol) and stirred overnight at room temperature. The product was concentrated and purified by preparative HPLC to yield the title compound as a mono-TFA salt (125 mg, 94% purity). MS m/z: [M+H]+ calcd for C18H23NO2, 286.17. found 286.2.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08853255B2
出典データセットuspto-grants-2014_10
ORD IDord-f75c8874f2fc43f2b07c0d3fe5cb7e7b
出典メモuspto-grants-2014_10