HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylene Glycol → 3-(1,3-Dioxolan-2-yl)isoquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Isoquinoline-3-carboxaldehyde | HCID 231555 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3-(1,3-Dioxolan-2-yl)isoquinoline | HCID 19047499 | 89.9% |
Reaction Steps
A mixture of 3-isoquinolinecarboxaldehyde (7 g, 44.5 mmol), 5.5 g (88 mmol) of ethylene glycol, 400 ml of toluene and 1.1 g (4.4 mmol) of p-toluenesulfonic acid was refluxed for 16 h while separating the water formed. The mixture was cooled to room temperature and washed with sodium bicarbonate solution, water, and brine. The organic layer was dried over sodium sulfate, and concentrated in vacuo to afford 8 g (89.9%) of 3-(1,3-dioxolan-2-yl)isoquinoline (Formula XII: R2 =R7 =H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05554620 |
| Source dataset | uspto-grants-1996_09 |
| ORD ID | ord-e24d34f2b92f429e9881db870ca1cd5f |
| Source note | uspto-grants-1996_09 |