Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 13088162 | HCID 13088162 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 14008100 | HCID 14008100 | — |
Reaction Steps
A mixture of 6-bromo-2-p-tolyl-benzo[de]isoquinoline-1,3-dione (4.0 g), sodium hydroxide (0.65 g), and 1,2-ethylene glycol (50 ml) was maintained under reflux with stirring at 120° C. for 10 hrs. The reaction mixture was then cooled to room temperature and water (100 ml) was added to the mixture. The solid that separated out was filtered, washed with water, and dried at 100° C. for 8 hours (Yield=2.71 g). The crude product was purified using 120 ml monochlorobenzene and 0.25 g activated charcoal to obtain pure product weighing 1.32 g. H1-NMR: 2.39 δ (s, 3 protons); 3.92 δ (m, 2 proton); 4.35 δ (t, 2 protons); 5.13 δ (t, 1 proton); 7.22 δ (m, 2 protons); 7.31 δ (m, 3 protons); 7.83 δ (t, 1 proton); 8.44 δ (m, 2 protons); 8.68 δ (d, 1 proton).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08183310B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-65ccd2d78d054f14a6a5ad609071a9e5 |
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| Source note | uspto-grants-2012_05 |
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