戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 896802作成日:2026年10月25日

Triethylamine → [(4-Methoxyphenyl)hydrazono]acetic acid ethyl ester

https://huagongshe.com/reaction/896802

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物4-Methoxyphenylhydrazine hydrochlorideHCID 2723904—
反応物Alpha-HydroxybutyrateHCID 4071895—
溶媒TolueneHCID 1140—
溶媒TetrahydrofuranHCID 8028—
生成物[(4-Methoxyphenyl)hydrazono]acetic acid ethyl esterHCID 6944586290%

反応条件

温度2.5 °C

反応手順

A suspension of 4-methoxy-phenylhydrazine hydrochloride (32, 14.0 g, 80.2 mmol) in anhydrous THF (100 mL) was treated with triethylamine (TEA, 8.10 g, 11.2 mL, 80.2 mmol, 1.0 equiv) before a solution of ethylglycolate (50% solution in toluene, 16.4 g, 80.2 mmol, 1.0 equiv) in toluene was dropwise added into the reaction mixture at 0-5° C. under N2. The resulting reaction mixture was then stirred at 0-5° C. for 30 min before being gradually warmed to 25° C. for 12 h. When TLC and HPLC showed the reaction was deemed complete, the reaction mixture was filtered to collect triethylamine hydrochloride salt. The filtrates were concentrated in vacuo, and the resulting solids were collected by filtration. The crude solids were washed with water (2×50 mL) and 20% of EtOAc/hexane (2×50 mL), and dried at 40-45° C. in vacuo for 12 h to afford the crude, desired [(4-methoxyphenyl)hydrazono]acetic acid ethyl ester (33, 16.0 g, 17.80 g theoretical, 90%), which was found to be pure enough to do the following reaction without further purification. For 33: CIMS m/z 221 (M+−H, C11H14N2O3).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06919451B2
出典データセットuspto-grants-2005_07
ORD IDord-b23ad070141443c09f1b914aa61cd286
出典メモuspto-grants-2005_07