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HRID 1608549作成日:2026年10月25日

Dimethylformamide → HCID 53789916、化合物

https://huagongshe.com/reaction/1608549

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物OctadecylamineHCID 15793—
反応物Thionyl ChlorideHCID 24386—
反応物Cinnamic acid, p-hydroxy-, acetateHCID 85857—
溶媒ChloroformHCID 6212—
溶媒TriethylamineHCID 8471—
生成物HCID 53789916HCID 5378991678%

反応手順

Under a nitrogen atmosphere, 4-acetoxycinnamic acid (150 g) and N,N-dimethylformamide (5 ml) were suspended in chloroform (800 ml) and thereto was added dropwise thionyl chloride (104 g) over a period of about 30 minutes. After completion of the addition, the reaction mixture was reflexed with heating for 1 hour to prepare the corresponding acid chloride. The reaction mixture was cooled to room temperature and thereto was added dropwise a solution of octadecylamine (196 g) and triethylamine (81 g) in chloroform (50 ml) over a period of about 30 minutes, followed by refluxing with heating for 3 hours. The reaction mixture was cooled to room temperature to precipitate a white crystal, which was filtered off under reduced pressure and dried to obtain N-octadecyl-p-acetoxycinnamamide (258 g). Yield 78%. This was suspended in 1,4-dioxane (1200 ml) and thereto was added aqueous KOH solution 50%; 127 g) and the reaction was allowed to proceed at 40°-45° C. for 24 hours. After completion of the reaction, the reaction mixture was cooled to room temperature to precipitate a white crystal, which was filtered off under reduced pressure. This crystal was washed with distilled water and recrystallized from methanol to obtain the desired product (211 g). Yield 90%; m.p. 114° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05395815
出典データセットuspto-grants-1995_03
ORD IDord-ebae5944d4514dcc8cff4dc664439ce1
出典メモuspto-grants-1995_03