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HRID 52487作成日:2026年10月26日

Chlorotrimethylsilane → N-ethoxalyl-2-trimethylsilyloxymethyltetrahydroquinoline

https://huagongshe.com/reaction/52487

反応式

関与物質

役割名称HCID仕込み量
反応物ChlorotrimethylsilaneHCID 6397—
反応物TriethylamineHCID 8471—
反応物Ethoxalyl chlorideHCID 20884—
反応物(1,2,3,4-Tetrahydroquinolin-2-yl)methanolHCID 15052240—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物N-ethoxalyl-2-trimethylsilyloxymethyltetrahydroquinolineHCID 67722031106%

反応条件

温度0 °C

反応手順

To a solution of 2-hydroxymethyltetrahydroquinoline (7.86 g, 48.16 mmol) in dichloromethane (80 mL) containing triethylamine (10 mL, 72.23 mmol) was added trimethylsilyl chloride (6.7 mL, 52.97 mmol) at 0° C. The mixture was stirred for 10 min at 0° C. followed by addition of triethylamine (10 mL) and ethyl chlorooxalate (5.9 mL, 52.97 mmol). The mixture was stirred for 30 min at 0° C. and water was added. The organic layer was separated, washed with water, dried over magnesium sulfate, and concentrated to give 15.6 g of N-ethoxalyl-2-trimethylsilyloxymethyltetrahydroquinoline (106%): 1H NMR (270 MHz, CDCl3) δ6.97~7.16 (m, 4H), 4.68 (m, 1H), 4.09 (q, 2H, J=7 Hz), 3.72 (m, 1H), 3.54 (m, 1H), 2.65 (m, 2H), 2.37 (m, 1H), 1.69 (m, 1H), 1.06 (t, 3H, J=7 Hz), 0.03 (s, 9H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05616586
出典データセットuspto-grants-1997_04
ORD IDord-d945c2c0c67642de846b24ce3050e7a9
出典メモuspto-grants-1997_04