HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 9H-Indeno[1,2-b]pyrazine-2,3,9(1H, 4H)-trione 9-ethylene dithioacetal
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | 1,2-Ethanedithiol | HCID 10902 | — |
| Reactant | 9H-Indeno[1,2-b]pyrazine-2,3,9(1H,4H)-trione | HCID 19035977 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 9H-Indeno[1,2-b]pyrazine-2,3,9(1H, 4H)-trione 9-ethylene dithioacetal | HCID 86749111 | — |
Reaction Steps
A suspension of 9H-indeno[1,2-b]pyrazine-2,3,9(1H, 4H)-trione. 0.9 H2O (2.0 g, 8.68 mmol) in toluene (50 ml), 1,2-ethanedithiol (2.19 ml, 26.04 mmol) and boron trifluoride etherate (1.07 ml, 8.68 mmol) was refluxed for 20 hours. The reaction mixture was cooled to room temperature, and the precipitate was filtered off and washed with toluene, ethanol-water (2:1) and ethanol. The crude material (2.40 g) was recrystallized from DMF-water to give 2.09 g (83%) of the title, compound. M.p.>300° C. 1H-NMR (DMSO-d6, δ): 3.68 (m, 2H), 3.91 (m, 2H), 7.2 (t, 1H), 7.3 (t, 1H), 7.51 (d, 1H), 7.59 (d, 1H), 12.05 (s, 1H), 12.38 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05646146 |
| Source dataset | uspto-grants-1997_07 |
| ORD ID | ord-c67660fa133f4f72b92c003fc573e3aa |
| Source note | uspto-grants-1997_07 |