戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 22131作成日:2026年10月23日

Triethylamine → 6-(4-(2-(2,4,6-Trimethylbenzenesulphonylamino)ethyl)phenyl)-6-(3-pyridyl)hex-5-enoic acid

https://huagongshe.com/ja/reaction/22131

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物2-Mesitylenesulfonyl chlorideHCID 13046—
反応物Methyl 6-(4-(2-aminoethyl)phenyl)-6-(3-pyridyl)hex-5-enoateHCID 54161160—
溶媒DichloromethaneHCID 6344—
生成物6-(4-(2-(2,4,6-Trimethylbenzenesulphonylamino)ethyl)phenyl)-6-(3-pyridyl)hex-5-enoic acidHCID 54316826—

反応手順

A mixture of 3.24 g of methyl 6-(4-(2-aminoethyl)phenyl)-6-(3-pyridyl)hex-5-enoate, 2.2 g of 2,4,6-trimethylbenzenesulphonic acid chloride and 100 ml of triethylamine in 50 ml of dichloromethane is stirred for 30 minutes at ambient temperature. Then the reaction mixture is washed twice with water, dried and evaporated down. The residue is purified over a silica gel column using ethyl acetate. The crude product obtain is heated in a mixture of 32 ml of ethanol and 5 ml of 4N sodium hydroxide solution for 30 minutes to 50° to 60° C. The reaction mixture is evaporated down, the residue is taken up in 50 ml of water and washed with ethyl acetate. The aqueous phase is adjusted to pH 5 by the addition of citric acid and extracted twice with ethyl acetate. The organic phase is dried, evaporated down and the residue is chromatographed over a silica gel column using ethyl acetate. The crude product is then recrystallised from ethyl acetate/diisopropyl ether.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05426119
出典データセットuspto-grants-1995_06
ORD IDord-7df537ef2af54ad2b761aab6a318ec77
出典メモuspto-grants-1995_06