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HRID 1765979作成日:2026年10月25日

Chlorotrimethylsilane → 2-(4-(N-salicyloyl)aminophenyl)propionic acid

https://huagongshe.com/reaction/1765979

反応式

関与物質

役割名称HCID仕込み量
反応物ChlorotrimethylsilaneHCID 6397—
反応物TriethylamineHCID 8471—
反応物4-Aminohydratropic acidHCID 43026—
反応物2-Acetoxybenzoyl chlorideHCID 79668—
溶媒DichloromethaneHCID 6344—
生成物2-(4-(N-salicyloyl)aminophenyl)propionic acidHCID 981730352.4%

反応条件

温度0 °C

反応手順

A slurry of 58.6 g (0.355 mol) of 2-(4-aminophenyl)propionic acid and 500 ml of methylene chloride is treated with 90.11 ml (77.13 g. 0–710 mol) of trimethylsilyl chloride and is heated to reflux for 120 min. The reaction mixture is cooled to 0° C. and treated with 184.44 ml (107.77 g, 1.065 mol) of triethylamine. After stirring for 5 minutes, this mixture is treated with a solution of 70.45 g (0.355 mol) of O-acetylsalicyloyl chloride and 150 ml of methylene chloride. The reaction mixture is warmed to 25° C. and stirred for 64 hr. The volatiles are removed in vacuo. The residue is stirred in 2N aqueous sodium hydroxide for one hour and acidified with 2 M aqueous sulfuric acid. The solid is recrystallized twice from ethanol/water to give a tan solid. Isolation by filtration results in an expected yield of 53.05 g (52% yield) of 2-(4-(N-salicyloyl)aminophenyl)propionic acid. Properties. Solubility: 200 mg/m: 200 mg+350 .μL 2N NaOH+650 .μL H2O-pH-7.67. Analysis: C, 67.36; H, 5.3; N,4.91.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07229966B2
出典データセットuspto-grants-2007_06
ORD IDord-2f9a217976e54ad3a663a832cb2f75ed
出典メモuspto-grants-2007_06