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HRID 2179144作成日:2026年10月27日

Indole → 1-(2-Methoxyphenyl)-1H-indole

https://huagongshe.com/reaction/2179144

反応式

関与物質

役割名称HCID仕込み量
反応物IndoleHCID 798—
反応物o-IodoanisoleHCID 68257—
生成物1-(2-Methoxyphenyl)-1H-indoleHCID 2827514100%

反応手順

Using general procedure A, indole (146 mg, 1.25 mmol)) was coupled with 2-iodoanisole (135 μL, 1.04 mmol). The crude product was purified by flash chromatography on silica gel (2×15 cm; hexane-ether 15:1; 15 mL fractions). Fractions 6-10 provided 232 mg (100% yield) of the product as a colorless oil. The 1H NMR spectrum was in accord with that reported by Maiorana et al. Maiorana, S.; Baldoli, C.; Del Buttero, P.; Di Ciolo, M.; Papagni, A. Synthesis 1998, 735.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09067955B2
出典データセットuspto-grants-2015_06
ORD IDord-0693a2bc7d214c68af9308ded9a7ca50
出典メモuspto-grants-2015_06