HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → HCID 17896911, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 5,6-Dihydroindeno[2,1-b]indole | HCID 13129410 | — |
| Catalyst | Hexadecyltrimethylammonium Bromide | HCID 5974 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 17896911 | HCID 17896911 | 37% |
Reaction Steps
In a 0.5 l bulb were placed 100 ml 50% aqueous NaOH, 100 ml benzene, 6.1 g (28 mmol)of 5,6-dihydroindeno[2,1-b]indole, prepared in Example 4, 5 g (41 mmol) of allyl-bromide and 0.5 g of trimethylcetylammonium bromide. After having stirred the obtained mixture for 12 hours, the formation of an organic phase was observed; said phase was separated, washed twice with water (100 ml) and dried over Na2SO4. After removal of the solvent, the residue was passed through a column of silicagel, eluted with hexane/ethylacetate=5:1); the resulting solution was evaporated, obtaining 1.8 g of N-allyl-5,6-dihydroindeno[2,1-b]indole (yield=37%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06451724B1 |
| Source dataset | uspto-grants-2002_09 |
| ORD ID | ord-ae87bebf6ca440a494c85c3ae9f11f1d |
| Source note | uspto-grants-2002_09 |