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HRID 344936作成日:2026年10月26日

Diisopropylamine → 6-Ethynyl-4,4-dimethylthiochroman

https://huagongshe.com/reaction/344936

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylamineHCID 7912—
反応物Diethyl chlorophosphateHCID 13139—
反応物Lithium diisopropylamideHCID 2724682—
反応物1-(4,4-Dimethylthiochroman-6-yl)ethanoneHCID 11708355—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
溶媒HexaneHCID 8058—
生成物6-Ethynyl-4,4-dimethylthiochromanHCID 10932539—

反応条件

温度-78 °C

反応手順

To a solution of 1.441 g (14.2405 mmol) of diisopropylamine in 30 ml dry tetrahydrofuran under argon at -78 degrees C. was added dropwise 9 ml of 1.6M (14.4 mmol) n-butyl lithium in hexane. After stirring this solution at -78 degrees C. for 1 hour, it was treated dropwise with a solution of 2.95 g (13.389 mmol) of 4,4-dimethyl-6-acetyl-thiochroman (Compound 62) in 5 ml of dry tetrahydrofuran. After another hour of stirring at -78 degrees C., the solution was treated with 2.507 g (14.53 mmol) of diethyl chlorophosphate and brought to room temperature, where it was stirred for 3.75 hours. This solution was then transferred using a double ended needle to a solution of lithium diisopropylamide [prepared using 2.882 g (28.481 mmol) of diisopropylamine and 18 ml of 1.6M (28.8 mmol) n-butyllithium in hexane] in 60 ml dry tetrahydrofuran at -78 degrees C. The cooling bath was removed and the solution stirred at room temperature for 15 hours, then quenched with water and acidified to pH 1 with 3N hydrogen chloride. The mixture was extracted with 5×50 ml pentane and the combined organic fractions washed with 3N hydrogen chloride, water, saturated NaHCO3 and saturated NaCl, then dried (MgSO4). Solvent was then removed in vacuo, and the residue purified by kugelrohr distillation (100 degrees C., 0.7 mm) to give the title compound as a pale yellow solid. PMR (CDCl3): & 1.34 (6H, s), 1.94-1.99 (2H, m), 3.04-3.08 (3H, m), 7.06 (1H, d, J~8.4 Hz), 7.17 (1 H, dd, J~8.4 Hz, 2.1 Hz), 7.51 (1H, d, J~2.1 Hz).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05053523
出典データセットuspto-grants-1991_10
ORD IDord-836173e05f624f90aedfda71245de747
出典メモuspto-grants-1991_10