反应 #543556

反应方程式

2-(4-aminophenyl)propionic acid

trimethylsilyl chloride

O-acetylsalicyloyl chloride

triethylamine

→

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

收率 52.4%

溶剂

methylene chloride

methylene chloride

反应条件

后处理

1. 1
   温度is heated
2. 2
   温度to reflux for 120 min
3. 3
   温度The reaction mixture is warmed to 25° C.
4. 4
   workup.STIRRINGstirred for 64 hr
5. 5
   其他The volatiles are removed in vacuo
6. 6
   workup.STIRRINGThe residue is stirred in 2N aqueous sodium hydroxide for one hour
7. 7
   其他The solid is recrystallized twice from ethanol/water
8. 8
   其他to give a tan solid
9. 9
   过滤Isolation by filtration

实验过程

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.

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