Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenol | HCID 996 | — |
| Reactant | Ethylenediamine | HCID 3301 | — |
| Reactant | 9-Chloroacridine | HCID 71013 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 86640754 | HCID 86640754 | 53% |
Reaction Steps
A mixture of 9-chloroacridine (1.21 g, 5.7 mmol) and phenol (10.8 g, 57 mmol) was mixed and heated at 110° C. for 45 min under argon. Distilled ethylene diamine (3.4 g, 57 mmol) was added via syringe. After the reaction mixture was heated at 110° C. for additional 2 hrs, it was poured into 2N NaOH solution (60 mL). The product was extracted with ethyl ether (3×100 mL). The combined organic layer was washed with 2N NaOH solution (40 mL) and water (2×100 mL) and dried with anhydrous potassium carbonate. The solution was concentrated to 15 mL. Ethanol (15 mL) was added, followed by the addition of concentrated hydrochloric acid (10 mL). The mixture was cooled in freezer (−20° C.) for 4 hrs. The yellow solid formed was collected by centrifugation, washed with ethyl ether (10 mL) and dried under vacuum to provide Compound 7 as yellow powder 0.82 g (53%) which was used without any further purification. The structure of Compound 7 is given below:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09250249B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-4a616171de7b46d29a009f39bd460a40 |
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| Source note | uspto-grants-2016_02 |
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