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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 479017Generated: October 25, 2026

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

https://huagongshe.com/reaction/479017

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantTriethylamineHCID 8471—
Reactant4-Aminohydratropic acidHCID 43026—
Reactant2-Acetoxybenzoyl chlorideHCID 79668—
SolventDichloromethaneHCID 6344—
Product2-(4-(N-salicyloyl)aminophenyl)propionic acidHCID 981730352.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

A slurry of 58.6 g (0.355 mol) of 2-(4-aminophenyl)propionicacid and 500 ml of methylene chloride was treated with 90.11 ml (77.13 g, 0-710 mol) of trimethylsilyl chloride and was heated to reflux for 120 min. The reaction mixture was 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 was treated with a solution of 70.45 g (0.355 mol) of O-acetylsalicyloyl chloride and 150 ml of methylene chloride. The reaction mixture was warmed to 25° C. and stirred for 64 hr. The volatiles were removed in vacuo. The residue was stirred in 2N aqueous sodium hydroxide for one hour and acidified with 2 M aqueous sulfuric acid. The solid was recrystallized twice from ethanol/water to give a tan solid. Isolation by filtration afforded 53.05 g of (52% yield) of 2-(4-(N-salicyloyl)aminophenyl)propionic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06642411B1
Source datasetuspto-grants-2003_11
ORD IDord-1ae6f0b86b0f4478bba672050e38a6c8
Source noteuspto-grants-2003_11