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HRID 235689作成日:2026年10月26日

Dimethylformamide → 1-Hydroxy-3-[4-(tetradecyloxy)phenyl]-2-propanone

https://huagongshe.com/reaction/235689

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Oxalyl chlorideHCID 65578—
反応物p-Tetradecyloxyphenylacetic acidHCID 10472964—
溶媒DichloromethaneHCID 6344—
生成物1-Hydroxy-3-[4-(tetradecyloxy)phenyl]-2-propanoneHCID 20219109—

反応条件

温度95 °C

反応手順

To a suspension of about 60.0 g of (4-tetradecyloxyphenyl)acetic acid in about 400 ml of methylene chloride containing about 0.63 ml of dimethylformamide was added, over about 10 minutes about 27.31 g of oxalyl chloride. After about 2 hours the solvent was removed, the residue was dissolved in hexane and filtered through celite. The solvent was removed and the residue dried in vacuo. An about 110.82 g portion of tris-trimethylsilyloxyethylene was added and the solution was heated at about 95° C., under argon, for about 5 hours. The solution was poured into a mixture of about 30 ml of concentrated hydrochloric acid (about 12N) about 170 ml of water and about 200 ml of tetrahydrofuran with stirring and heat. This mixture was refluxed about 10 minutes, ethyl acetate was added, the warm organic layer separated and washed with brine, saturated sodium bicarbonate solution, then brine, dried and the solvent removed, giving, after recrystallization from hexane, about 52 g of the desired title compound as a white solid, mp. 84°-85° 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-4da355b1c1e34f2496e38f104615b413
出典メモuspto-grants-1987_02