HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1822346Generated: October 31, 2026
Potassium Carbonate → HCID 57894155, compound
https://huagongshe.com/reaction/1822346
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | HCID 57894228 | HCID 57894228 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 57894155 | HCID 57894155 | 84% |
Reaction Steps
A solution of 4-chloro-2-(2-fluoro-phenoxy)-benzaldehyde (0.8 g, 3.2 mmol) in chloroform (10 mL) is treated with m-CPBA (2.75 g, 16 mmol). The reaction is heated to reflux and stirred for about 2 hr. The reaction is cooled to room temperature and quenched with 10% aqueous NaHSO4. The aqueous is extracted with diethyl ether. The organic is washed with brine, dried over sodium sulfate, and the solvent is removed. The crude is diluted in methanol (20 mL) and treated with potassium carbonate (1.32 g, 9.6 mmol). The reaction stirred for 30 minutes at room temperature. The reaction is filtered and the solvent removed. The crude is purified by silica gel column chromatography using 4:1 hexanes:acetone to elute the pure product. The solvent is removed to afford about 0.64 g (84%) of product. 1H NMR (400 MHz, CDCl3). MS (ES−) m/z mass calcd for C12H8ClFO2 238, found 237 (M−1, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07608639B2 |
|---|
| Source dataset | uspto-grants-2009_10 |
|---|
| ORD ID | ord-7a1cead1ab7b44fcabc77ffc91b5b183 |
|---|
| Source note | uspto-grants-2009_10 |
|---|