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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1627746Generated: November 1, 2026

Water → 6-Bromo-8,8-dimethyl-8H-indolo[3,2,1-de]acridine

https://huagongshe.com/reaction/1627746

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantN-bromobutanimideHCID 67184—
Reactant8,8-dimethyl-8H-indolo[3,2,1-de]acridineHCID 12555402—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
Product6-Bromo-8,8-dimethyl-8H-indolo[3,2,1-de]acridineHCID 67109735—

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 8 g (45.1 mmol) of NBS in 100 ml of acetonitrile is subsequently added dropwise at −15° C. with exclusion of light, and the mixture is allowed to come to room temperature and is stirred at this temperature for a further 4 h. 150 ml of water are subsequently added to the mixture, which is then extracted with CH2Cl2. The organic phase is dried over MgSO4, and the solvents are removed in vacuo. The product is washed by stirring with hot hexane and filtered off with suction. Yield: 4.5 g (12 mmol), 57% of theory, purity according to 1H-NMR about 97%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785636B2
Source datasetuspto-grants-2014_07
ORD IDord-b1e5fb8dd18d4714a5f950853e05ce8b
Source noteuspto-grants-2014_07