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HRID 235712作成日:2026年10月27日

1-Iodooctadecane → N-[1-[(octadecyloxy)methyl]-2-[(tetrahydro-2H-pyran-2-yl)oxy]ethyl]acetamide

https://huagongshe.com/reaction/235712

反応式

関与物質

役割名称HCID仕込み量
反応物1-IodooctadecaneHCID 12402—
反応物Sodium hydrideHCID 24758—
反応物N-[1-(hydroxymethyl)-2-[(tetrahydro-2H-pyran-2-yl)oxy]ethyl]acetamideHCID 20219052—
溶媒Diethyl EtherHCID 3283—
溶媒DimethylformamideHCID 6228—
溶媒TetrahydrofuranHCID 8028—
生成物N-[1-[(octadecyloxy)methyl]-2-[(tetrahydro-2H-pyran-2-yl)oxy]ethyl]acetamideHCID 2021864934.1%

反応手順

A solution of about 10.85 g of N-[1-(hydroxymethyl)-2-[(tetrahydro-2H-pyran-2-yl)oxy]ethyl]acetamide in about 240 ml of dry dimethylformamide was added dropwise to a suspension of about 3.12 g of about 50% sodium hydride (pre-washed with anhydrous ether). After stirring about one hour a solution of about 22.8 g of octadecyl iodide in about 150 ml of tetrahydrofuran was added, stirring was continued for about 24 hours, then the mixture was diluted with ether and washed with a minimum amount of brine. The organic layer was dried, the solvents evaporated and the crude material purified by chromatography on silica gel, eluting with ethyl acetate:hexane:ethanol (about 1:1:0.2), giving about 8 g of the desired title compound, mp 52°-55° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04640913
出典データセットuspto-grants-1987_02
ORD IDord-ad0c1099a691405d99372083342fd252
出典メモuspto-grants-1987_02