HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylene Glycol → 3-(1,3-Dioxolan-2-yl)-2-fluoro-4-iodopyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 2-Fluoro-4-iodopyridine-3-carbaldehyde | HCID 9992328 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3-(1,3-Dioxolan-2-yl)-2-fluoro-4-iodopyridine | HCID 22744998 | — |
Reaction Steps
In a three-necked flask equipped with a Dean Stark apparatus, a mixture of 5.1 g (20.3 mmol) of 2-fluoro-4-iodo-3-pyridinecarbaldehyde, 1.4 g (22.3 mmol) of ethane-1.2-diol, and 50 mg of para-toluenesulphonic acid in 100 ml of toluene is heated at reflux. When the theoretical amount of water has been collected, the reaction mixture is cooled to room temperature, washed with a saturated sodium hydrogen carbonate solution and dried over magnesium sulphate. The expected product is obtained by concentration.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06509345B2 |
| Source dataset | uspto-grants-2003_01 |
| ORD ID | ord-4c3cb04e8cbc4d798cdb818161b234b1 |
| Source note | uspto-grants-2003_01 |