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HRID 16567作成日:2026年10月25日

Imidazole → 4-(t-Butyldimethylsilyloxy)indole

https://huagongshe.com/reaction/16567

反応式

関与物質

役割名称HCID仕込み量
反応物ImidazoleHCID 795—
反応物tert-Butyldimethylsilyl chlorideHCID 28928—
反応物1H-indol-4-olHCID 75421—
溶媒DichloromethaneHCID 6344—
生成物4-(t-Butyldimethylsilyloxy)indoleHCID 11593976113.3%

反応手順

A solution of 4-hydroxyindole (13.31 g, 75 mmol) in dry dichloromethane (400 mL) was treated with imidazole (8.17 g, 120 mmol) and t-butyldimethylsilyl chloride (18.09 g, 120 mmol) and the mixture was stirred at room temperature under nitrogen overnight. The precipitated white solid was filtered off and washed with dichloromethane and the combined filtrates were washed successively with 0.5 M aq. hydrochloric acid, 0.5 M aq. sodium hydroxide and brine, dried and evaporated to give 9 as white crystals (21.03 g, 85%), mp 80-81° C. (from hexanes); 1H NMR (500 MHz) δ 8.06 (br s, 1H), 7.08 (dd, J=3.1, 2.4 Hz, 1H), 6.99-7.05 (m, 2H), 6.58-6.59 (m, 1H), 6.52 (dd, J=7, 1.5 Hz, 1H, 1.06 (s, 9H), 0.23 (s, 6H). Anal. Calcd. for C14H21NOSi: C, 67.97; H, 8.56; N, 5.66. Found: C, 67.60; H, 8.80; N, 5.57.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07737169B2
出典データセットuspto-grants-2010_06
ORD IDord-cafe1f939f3a4c769dbba9559b0274bf
出典メモuspto-grants-2010_06