戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 35260作成日:2026年10月24日

Triethylamine → N-ethyl-N-cyclohexyl-5-(1-cyclohexyl-1,2,3,4-tetrazol-5-yl)valeramide

https://huagongshe.com/ja/reaction/35260

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物N-Ethyl cyclohexylamineHCID 21609—
反応物Isobutyl chloroformateHCID 62365—
反応物5-(1-Cyclohexyl-1,2,3,4-tetrazol-5-yl)valeric acidHCID 13203402—
溶媒TetrahydrofuranHCID 8028—
生成物N-ethyl-N-cyclohexyl-5-(1-cyclohexyl-1,2,3,4-tetrazol-5-yl)valeramideHCID 1320339772.6%

反応手順

5-(1-Cyclohexyl-1,2,3,4-tetrazol-5-yl)valeric acid (2.5 g) is dissolved in tetrahydrofuran (50 ml), and thereto is added triethylamine (1.1 g). To the mixture is added dropwise with stirring isobutyl chloroformate (1.5 g) under ice-cooling, and the mixture is stirred at room temperature for 30 minutes. To the mixture is added dropwise with stirring N-ethyl-cyclohexylamine (1.5 g) at room temperature, and the mixture is further stirred for 2 hours. After distilling off tetrahydrofuran, water is added to the residue, and the mixture is extracted with chloroform. The chloroform layer is washed with an aqueous saturated sodium chloride solution and dried over magnesium sulfate. Chloroform is distilled off, and the resulting residue is subjected to column chromatography (Kieselgel 60, made by Merck & Co., eluting solvent, chloroform) to isolate N-ethyl-N-cyclohexyl-5-(1-cyclohexyl-1,2,3,4-tetrazol-5-yl)valeramide (2.6 g), white crystalline powder (ether), m.p. 92°-95° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04766120
出典データセットuspto-grants-1988_08
ORD IDord-25fc57d6c3534e629f1814f0d825248e
出典メモuspto-grants-1988_08