HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1097432Generated: October 31, 2026
Potassium Iodide → Benzyl N-(2-oxo-2,3-dihydro-1H-indol-4-yl)glycinate
https://huagongshe.com/reaction/1097432
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | Benzyl bromoacetate | HCID 62576 | — |
| Reactant | 4-Aminoindolin-2-one | HCID 12237472 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Benzyl N-(2-oxo-2,3-dihydro-1H-indol-4-yl)glycinate | HCID 66813100 | — |
Reaction Steps
A mixture of 4-amino-1,3-dihydro-2H-indol-2-one (300 mg, 2.03 mmol), benzyl bromoacetate (0.32 mL, 2.03 mmol), cesium carbonate (660 mg, 2.03 mmol), and potassium iodide (336 mg, 2.03 mmol) in DMF (10 mL) was stirred at 50° C. for 4 h. The cooled reaction mixture was quenched with H2O (10 mL) and extracted with EtOAc (2×15 mL). The combined organic extracts were dried over Na2SO4, filtered, and concentrated in vacuo. The crude product was purified by silica gel chromatography, eluting with a gradient of CH2Cl2:EtOAc—100:0 to 80:20, to give the title compound. MS: m/z=297 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08143266B2 |
|---|
| Source dataset | uspto-grants-2012_03 |
|---|
| ORD ID | ord-5df8d1bb8a13430eae1f1734bafcf07b |
|---|
| Source note | uspto-grants-2012_03 |
|---|