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HRID 129536作成日:2026年10月27日

2-Dimethylaminopyridine → HCID 178520426、化合物

https://huagongshe.com/reaction/129536

反応式

関与物質

役割名称HCID仕込み量
反応物2-DimethylaminopyridineHCID 21885—
反応物Cyclohexanepropanoic acidHCID 69702—
反応物Potassium BromideHCID 253877—
反応物Tetronic acidHCID 521261—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
溶媒DimethylformamideHCID 6228—
溶媒TriethylamineHCID 8471—
生成物HCID 178520426HCID 178520426—

反応手順

To a solution of 2.0 g of tetronic acid in 40 ml of dry N,N-dimethylformamide was added (at 0° C.) 3.1 ml of triethylamine and 0.81 g of dimethylaminopyridine. After stirring for 5 minutes, 3.4 ml of 3-cyclohexylpropanoic acid was added, followed by 4.6 g of 1-(3-dimethylaminopropyl)-3-ethyl carbodiimide hydrochloride. After 10 minutes the ice bath is removed and the mixture is allowed to stir overnight. The reaction mixture is quenched with 1N hydrochloric acid and the solution is washed 3 times with hexanes. The combined organic layers are combined, washed with brine, dried over magnesium sulfate and evaporated to give a yellow solid, which is recrystallized from hexanes to give light yellow crystals: m.p. 75°-78° C.; IR (KBr) 2910, 2820, 1750, 1640, 1600 cm-1 ; NMR (CDCl3) δ 0.9-1.8 (1 1H, m), 2.9 (t, 2H, J=6 Hz), 4.7 and 4.5 (s, 2H (tautomers)); MS EI M+ 238.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05468774
出典データセットuspto-grants-1995_11
ORD IDord-1b443bad3e6b46e5ab539d1cb4d0abec
出典メモuspto-grants-1995_11