戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 279910作成日:2026年10月23日

Pyridine → HCID 54422056、化合物

https://huagongshe.com/ja/reaction/279910

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物TriclosanHCID 5564—
反応物Thionyl ChlorideHCID 24386—
反応物2-Hexadecanoyloxy-1-(hexadecanoyloxymethyl)ethyl hydrogen glutarateHCID 23322903—
溶媒CyclohexaneHCID 8078—
生成物HCID 54422056HCID 54422056—

反応条件

温度35 °C

反応手順

A mixture of cyclohexane (60 ml.), pyridine (1.43 ml.) and 2-hexadecanoyloxy-1-(hexadecanoyloxymethyl)ethyl hydrogen glutarate (B) (11.0 g.) was warmed to 35° C. The solution obtained was added dropwise during 45 minutes to a stirred solution of thionyl chloride (1.23 ml.) in cyclohexane (25 ml.) at 35° C. The mixture was then stirred for a further 1.5 hours at 35° C., cooled to 15° C. and a solution of triclosan (4.68 g.) and pyridine (1.56 ml.) in cyclohexane (20 ml.) added during 15 minutes. The mixture was stirred at ambient temperature for 16 hours, warmed to 35° C. and washed first with 0.5 M hydrochloric acid (100 ml.) and then with water (3×100 ml.), also heated to 35° C. The mixture was then dried (MgSO4) and evaporated to give 5-chloro-2-(2,4-dichlorophenoxy)phenyl 2-hexadecanoyloxy-1-(hexadecanoyloxymethyl)ethyl glutarate as a white solid, m.p. 44°-46° C., identical with the material obtained in Example 4 as judged by its NMR and mass spectral properties.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04587262
出典データセットuspto-grants-1986_05
ORD IDord-b9c7435022e044fba33b4ced42b2f2cc
出典メモuspto-grants-1986_05