戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 53227作成日:2026年10月24日

Triethylamine → 1-[4-(3-Trifluoromethylphenyl)-1,2,3,6-tetrahydropyrid-1-yl]-1-oxo-2-(6-methoxy-naphth-2-yl)ethane

https://huagongshe.com/ja/reaction/53227

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物6-Methoxy-2-naphthylacetic acidHCID 32176—
反応物Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
反応物4-(3-(Trifluoromethyl)phenyl)-1,2,3,6-tetrahydropyridine hydrochlorideHCID 23435991—
溶媒DichloromethaneHCID 6344—
生成物1-[4-(3-Trifluoromethylphenyl)-1,2,3,6-tetrahydropyrid-1-yl]-1-oxo-2-(6-methoxy-naphth-2-yl)ethaneHCID 1515688081%

反応手順

A solution of 6-methoxy-2-naphthylacetic acid (1.8 g, 0.009 mol), 4-(3-trifluoromethylphenyl)-1,2,3,6-tetrahydropyridine hydrochloride (2.4 g, 0.009 mol), triethylamine (2.4 ml, 0.018 mol), and BOP (3.7 g, 0.009 mol) in methylene chloride (40 ml) is stirred at room temperature for 5 hours. Then it is concentrated to dryness, the obtained residue is dissolved in a mixture ethyl ether/water, the organic phase is separated, and washed sequentially with 1N HCl, water, 5% NaOH, and water. The reaction mixture is then filtered over silica and the filtrate is concentrated to dryness affording 1-[4-(3-trifluoromethylphenyl)-1,2,3,6-tetrahydropyrid-1-yl]-1-oxo-2-(6-methoxy-naphth-2-yl)ethane (3.1 g). M.p. 102°-105° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05618822
出典データセットuspto-grants-1997_04
ORD IDord-f898c8d2b26d42d5bb499d3517a5fddd
出典メモuspto-grants-1997_04