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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 456374생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/456374

반응식

참여 물질

역할이름HCID투입량
반응물ChlorotrimethylsilaneHCID 6397—
반응물TriethylamineHCID 8471—
반응물4-Aminohydratropic acidHCID 43026—
반응물2-Acetoxybenzoyl chlorideHCID 79668—
용매DichloromethaneHCID 6344—
생성물2-(4-(N-salicyloyl)aminophenyl)propionic acidHCID 981730352.4%

반응 조건

온도0 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07186691B2
출처 데이터셋uspto-grants-2007_03
ORD IDord-90030ab3e14f4ae295ed31050ef8ba7f
출처 메모uspto-grants-2007_03