HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylene Glycol → HCID 178520159, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | HCID 178519714 | HCID 178519714 | — |
| Product | HCID 178520159 | HCID 178520159 | — |
Reaction Steps
1.3 mmol of cyclopropyl 4-(3-(1H-imidazol-4-yl)propyloxy)phenyl ketone (Example 61) and a catalytic amount of 4-toluenesulphonic acid in 15 ml of ethylene glycol are brought to reflux for 5 hours. The solvent is evaporated off under reduced pressure, and the residue is dissolved in 10 ml of H2O and alkalized with ammonia. The crude product is extracted with dichloromethane and purified by rotatory chromatography (eluent: dichloromethane/methanol (99:1-90:10), ammoniacal atmosphere). The product is crystallized in the form of hydrogen maleate from diethyl ether and ethanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06248765B1 |
| Source dataset | uspto-grants-2001_06 |
| ORD ID | ord-103e0edb335b4578a355c04e66ce9845 |
| Source note | uspto-grants-2001_06 |