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HRID 236481作成日:2026年10月26日

Hydrochloric Acid → N-[3-(Hexadecanoyloxy)octadecanoyl]-L-valine

https://huagongshe.com/reaction/236481

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物L-ValineHCID 6287—
反応物DicyclohexylcarbodiimideHCID 10868—
反応物N-HydroxysuccinimideHCID 80170—
反応物3-Hexadecanoyloxyoctadecanoic acidHCID 13489028—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
溶媒TriethylamineHCID 8471—
溶媒1,4-DioxaneHCID 31275—
生成物N-[3-(Hexadecanoyloxy)octadecanoyl]-L-valineHCID 5372993762.6%

反応手順

3-Hexadecanoyloxyoctadecanoic acid (10.8 g) prepared by the method described in Preparation A-2 (5) and N-hydroxysuccinimide (2.3 g) was dissolved in dioxane (60 ml). N,N'-Dicyclohexylcarbodiimide (4.2 g) was added thereto under ice cooling. The mixture was stirred at ambient temperature over-night. The crystallized N,N'-dicyclohexylurea was filtered off and the filtrate was concentrated to give a residue. The residue was dissolved in N,N-dimethylformamide (70 ml). To this solution was added a solution of L-valine (5.85 g) and triethylamine (6.95 ml) in water (50 ml) at 0° C. The resulting mixture was stirred at ambient temperature overnight. The reaction mixture was acidified with 1N hydrochloric acid, extracted with ethyl acetate, washed with water and dried over magnesium sulfate. Ethyl acetate was distilled off to give a residue which was crystallized from petroleum ether to give crystals of N-(3-hexadecanoyloxyoctadecanoyl)-L-valine (8 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04643990
出典データセットuspto-grants-1987_02
ORD IDord-8f9b83e64f3f4693b46e3b73e9a3fec2
出典メモuspto-grants-1987_02