HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 3-Bromo-8,8-dimethyl-8H-indolo[3,2,1-de]acridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 8,8-dimethyl-8H-indolo[3,2,1-de]acridine | HCID 12555402 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Bromo-8,8-dimethyl-8H-indolo[3,2,1-de]acridine | HCID 67109585 | — |
Reaction Steps
6.3 g (22.2 mmol) of 8,8-dimethylindolo[3,2,1-de]acridine are initially introduced in 150 ml of CH2Cl2. A solution of 3.9 g (22.3 mmol) of NBS in 100 ml of acetonitrile is subsequently added dropwise at −15° C. with exclusion of light, and the mixture is stirred at room temperature for a further 4 h. For work-up, 150 ml of water are added to the mixture, which is then extracted with CH2Cl2. The organic phase is dried over MgSO4, and the solvent is removed in vacuo. The product is washed by stirring with hot hexane and filtered off with suction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09133119B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-089a2f96f3eb435d9530107b036be6ad |
| Source note | uspto-grants-2015_09 |