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HRID 1006416作成日:2026年10月25日

Tetrabutylammonium Fluoride → 4-(4-Benzyl-piperazin-1-yl)-1H-indole

https://huagongshe.com/reaction/1006416

反応式

関与物質

役割名称HCID仕込み量
反応物Tetrabutylammonium FluorideHCID 2724141—
反応物1-triisopropylsilanyl-4-(4-benzyl-piperazin-1-yl)-1H-indoleHCID 22671261—
溶媒TetrahydrofuranHCID 8028—
生成物4-(4-Benzyl-piperazin-1-yl)-1H-indoleHCID 2728532—

反応手順

To a solution of 1.2 gram (2.68 mmole) 1-triisopropylsilanyl-4-(4-benzyl-piperazin-1-yl)-1H-indole in 20 mL tetrahydrofuran was added 3 mL (3 mmole) 1.0 M tetrabutylammonium fluoride in tetrahydrofuran. After 2 hours the solution was concentrated under reduced pressure and the residue was partitioned between 25 mL ethyl ether and 10 mL 10% sodium carbonate. The organic phase was washed with 3×10 mL water, dried (magnesium sulfate), and concentrated. 4-(4-Benzyl-piperazin-1-yl)-1H-indole was isolated as the white hydrochloride salt from ethyl ether, 604 mg, m.p. 233-234° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06790848B2
出典データセットuspto-grants-2004_09
ORD IDord-26dcf6bbf05a427292e269124172fdfc
出典メモuspto-grants-2004_09