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HRID 256564作成日:2026年10月27日

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

https://huagongshe.com/reaction/256564

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 (1.6 M, 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US05258379
出典データセットuspto-grants-1993_11
ORD IDord-38b33c1164ab486990b77e9053ff4e22
出典メモuspto-grants-1993_11