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HRID 1067904作成日:2026年10月25日

Diethyl Sulfate → tert-Butylisobutylethylamine

https://huagongshe.com/reaction/1067904

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl SulfateHCID 6163—
反応物HexaneHCID 8058—
反応物Potassium HydroxideHCID 14797—
反応物N-tert-butyl-2-methylpropan-1-amineHCID 527145—
反応物ButyllithiumHCID 178418339—
生成物tert-ButylisobutylethylamineHCID 438494172%

反応条件

温度70 °C

反応手順

A mixture of tert-butylisobutylamine (25.84 g, 0.2 mol) and diethyl sulfate (46.26 g, 0.3 mol) was warmed to 70° C. with stirring. An exothermic reaction started and in a few minutes the temperature rose to 150° C. with vigorous boiling of the mixture. After cooling to ˜50° C., 5 M aqueous potassium hydroxide (100 ml, 0.5 mol) was added. The organic layer was separated and dried over anhydrous magnesium sulfate. Diethyl sulfate (10 ml) was added and the mixture was stirred at 100° C. for 1 h. Aqueous 5 M potassium hydroxide (100 ml) was added and the mixture was stirred at 80° C. for 1 h. The organic layer was separated and the aqueous layer was extracted with diethyl ether (50 ml). The organic solutions were combined, dried over anhydrous magnesium sulfate and the product was isolated by distillation. A small amount (1-2%) of tert-butylisobutylamine which was removed by the addition of 2.5 M n-butyllithium in hexane (5.0 ml, 10 mmol) and the product distilled to yield 22.56 g, (72%) of product, bp 68-70° C./40 mm Hg; 1H NMR (CDCl3) δ0.85 (d, J=6.5 Hz, 6H, CH3), 0.98 (t, J=6.5 Hz, 3H, CH3), 1.01 (s, 9H, CH3), 1.66 (n, J=6.5 Hz, 1H, CH), 2.04 (d, J=6.57 Hz, 2H, CH2), 2.51 (q, J=6.5 Hz, 2H, CH2).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06248885B1
出典データセットuspto-grants-2001_06
ORD IDord-34b25f9e93fc43feb5b9c968548cab3e
出典メモuspto-grants-2001_06