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HRID 580603作成日:2026年10月27日

Morpholine → 4-Amino-beta-(4-chlorophenyl)-3,5-dichloro-cinnamic acid morpholide

https://huagongshe.com/reaction/580603

反応式

関与物質

役割名称HCID仕込み量
反応物MorpholineHCID 8083—
反応物TriethylamineHCID 8471—
反応物Ethyl chloroformateHCID 10928—
反応物4-Amino-beta-(4-chlorophenyl)-3,5-dichloro-cinnamic acidHCID 53943695—
溶媒ChloroformHCID 6212—
生成物4-Amino-beta-(4-chlorophenyl)-3,5-dichloro-cinnamic acid morpholideHCID 54521919—

反応条件

温度-10 °C

反応手順

20 g (0.058 mol) of 4-amino-β-(4-chlorophenyl)-3,5-dichloro-cinnamic acid (mixture of isomers A and B in the ratio 1:1.5) were dissolved in 700 ml of dry chloroform. 5.93 g (0.058 mol) of triethylamine were added while cooling with ice and stirring, and the mixture was cooled to -10° C. and combined with 6.35 g (0.058 mol) of ethyl chloroformate. After the addition had ended, 25.5 g (0.29 mol) of morpholine were added while further stirring and cooling. The resulting mixture was stirred for 4 hours more at room temperature and then extracted three times with water, and the organic phase was dried over sodium sulfate and concentrated to dryness in vacuo. The residue was chromatographed on a silica gel column (silica gel: substance=10:1, eluant: chloroform/ethyl acetate=1:1). The eluates containing substance were combined and evaporated to dryness in vacuo. Colorless crystals were obtained, melting point 140°-144° C., which contained the cis/trans isomer mixture in a proportion of 3:2.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04753934
出典データセットuspto-grants-1988_06
ORD IDord-4b56859e3dd44daca0e2020c3203dfc8
出典メモuspto-grants-1988_06