HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → HCID 66961793, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | Sodium bicarbonate water | HCID 86585896 | — |
| Reactant | HCID 86602483 | HCID 86602483 | — |
| Solvent | Ethylene Glycol | HCID 174 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 66961793 | HCID 66961793 | — |
Reaction Steps
To a toluene (70 mL) solution of 4-(1H-imidazol-1-yl-3-methoxybenzaldehyde (4.3 g) and ethylene glycol (6.5 g), para-toluenesulfonic acid monohydrate (4.8 g) was added, Dean-Stark equipment was attached and heat-refluxing was carried out for 4 hours. After allowing cool the reaction mixture to room temperature, a saturated sodium bicarbonate water and ethyl acetate were added, and the organic layer was partitioned. The organic layer was washed with a saturated salt solution and concentrated under reduced pressure after dried over anhydrous magnesium sulfate. The residue was purified by silica gel column chromatography (elution solvent: hexane-ethyl acetate system), and 3.15 g of the title compound was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07880009B2 |
| Source dataset | uspto-grants-2011_02 |
| ORD ID | ord-5ee04bd4cc9144bba437bf3349616bfe |
| Source note | uspto-grants-2011_02 |