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HRID 233947作成日:2026年10月26日

Hexane → 2-Dipropylamino-8-methylthio-1,2,3,4-tetrahydronaphthalene

https://huagongshe.com/reaction/233947

反応式

関与物質

役割名称HCID仕込み量
反応物HexaneHCID 8058—
反応物Dimethyl DisulfideHCID 12232—
反応物8-Bromo-2-dipropylamino-1,2,3,4-tetrahydronaphthaleneHCID 14529564—
反応物ButyllithiumHCID 178418339—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物2-Dipropylamino-8-methylthio-1,2,3,4-tetrahydronaphthaleneHCID 990373580.3%

反応条件

温度-78 °C

反応手順

To a solution of 8-bromo-2-di-n-propylamino-1,2,3,4-tetrahydronaphthalene (600 mg, 1.93 mMol) in tetrahydrofuran (20 mL) at -78° C. was added a solution of n-butyllithium in hexane (1.6M, 1.9 mL, 3.04 mMol). The solution was stirred at -78° C. for one hour, forming a light orange solution. Dimethyl disulfide (0.24 mL, 3.00 mMol) was added, and the reaction mixture was allowed to warm gradually to room temperature. The colorless solution was diluted with water and extracted with dichloromethane. The dichloromethane extracts were combined, dried (Na2SO4), and concentrated in vacuo to give the crude product as a light yellow oil. Purification by flash chromatography (3% methanol in dichloromethane + tr. NH4OH) gave the product as a colorless, viscous oil (430 mg, 80%). The hydrochloride salt was formed. Recrystallization (ethanol/diethyl ether) gave a colorless, crystalline solid (m.p.=185° C.).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05594034
出典データセットuspto-grants-1997_01
ORD IDord-4a7843a32e0d41108f74b3d1a6a3928b
出典メモuspto-grants-1997_01