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HRID 440349作成日:2026年10月25日

Fluorene → 2-(9H-fluoren-9-yl)ethane-1-thiol

https://huagongshe.com/reaction/440349

反応式

関与物質

役割名称HCID仕込み量
反応物FluoreneHCID 6853—
反応物ThiiraneHCID 9865—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物2-(9H-fluoren-9-yl)ethane-1-thiolHCID 2240702968.1%

反応手順

A solution of fluorene (20.0 g; 120 mmol) in THF (200 mL) was cooled to -40° C. and treated with 48 mL of a 2.5M solution of n-butyllithium in hexanes (120 mmol). After stirring for 15 minutes, a solution of ethylene sulfide (6.5 mL; 109 mmol) in 30 mL of THF was added, and the resulting mixture was stirred at -40° C. for 30 minutes and room temperature for 2 hours. The reaction was quenched by the addition of saturated ammonium chloride, the layers were separated, and the organic phase was washed with 10% HCl, dried and concentrated. The crude product was purified on a flash column, eluting with hexane, to provide 16.8 g (62%) of the product as an oil that recrystallized from hexane as a white solid, mp 38°-40° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05519043
出典データセットuspto-grants-1996_05
ORD IDord-d7ae73318a8c4e7c8630bf168d4ff67b
出典メモuspto-grants-1996_05