Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | 5-Methyl-5,6-dihydroindeno[2,1-b]indole | HCID 13129411 | — |
| Product | HCID 18424916 | HCID 18424916 | 90% |
Reaction Steps
21.9 g (0.1 mol) of N-methyl-5,6-dihydroindeno[2,1-b]indole, prepared in Example 5, and 200 ml of DMFA were placed into a bulb and the resulting mixture was heated under stirring to 50° C. 3.4 g (0.05 mol) of NaOEt were added to the mixture and the resulting solution was stirred for 10 minutes and then treated with 3.8 ml 37% formaline. The resulting mixture was stirred for 2 hours at 75° C.; then it was cooled to room temperature and treated with 5.3 g of NH4Cl. The precipitate was filtered, washed twice with DMFA (30 ml) and with ether, and finally dried thus yielding 20 g of the ligand 6-[(N-methyl-5,6-dihydroindeno[2,1-b]indol-6-yl)methyl]-N-methyl-5,6-dihydroindeno[2,1-b]indole (yield=90%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06451724B1 |
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| Source dataset | uspto-grants-2002_09 |
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| ORD ID | ord-1d9c9958c057494c9c27b1e89c1b0190 |
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| Source note | uspto-grants-2002_09 |
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