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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Aminohydratropic acid | HCID 43026 | — |
| Reactant | 2-Acetoxybenzoyl chloride | HCID 79668 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(4-(N-salicyloyl)aminophenyl)propionic acid | HCID 9817303 | 52.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06642411B1 |
|---|
| Source dataset | uspto-grants-2003_11 |
|---|
| ORD ID | ord-1ae6f0b86b0f4478bba672050e38a6c8 |
|---|
| Source note | uspto-grants-2003_11 |
|---|