HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylene Glycol → 3-[3-(1,3-Dioxolan-2-yl)phenoxy]propanamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | 3-(3-(1,3-Dioxoisoindolin-2-yl)propoxy)benzaldehyde | HCID 12810640 | — |
| Catalyst | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 3-[3-(1,3-Dioxolan-2-yl)phenoxy]propanamine | HCID 12797447 | 85% |
Reaction Steps
A solution of 2-[3-(3-formylphenoxy)propyl]-1H-isoindole-1,3-(2H)-dione (90 g) and p-toluenesulphonic acid, monohydrate (200 mg) in benzene (900 ml) and ethane-1,2-diol (25 g) was heated under reflux using a Dean-Stark separator for 8 h. The cooled solution was washed successively with sodium carbonate solution, water, sodium chloride solution, and evaporated in vacuo. The resulting oil was dissolved in tetrahydrofuran (1 liter) and stirred with hydrazine hydrate (50 ml) at room temperature for 24 hr. The mixture was diluted with ether and filtered. The filtrate was distilled to give the title compound as a colourless oil (55.2 g) b.p. 134°-6° (0.7 mm). TLC silica; methanol:ammonia 80:1; Rf 0.4.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04442110 |
| Source dataset | uspto-grants-1984_04 |
| ORD ID | ord-def86e0895e9498a9071a9f3791cb42f |
| Source note | uspto-grants-1984_04 |