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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2277342Generated: October 29, 2026

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

https://huagongshe.com/reaction/2277342

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantN-bromobutanimideHCID 67184—
Reactant8,8-dimethyl-8H-indolo[3,2,1-de]acridineHCID 12555402—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
Product3-Bromo-8,8-dimethyl-8H-indolo[3,2,1-de]acridineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133119B2
Source datasetuspto-grants-2015_09
ORD IDord-089a2f96f3eb435d9530107b036be6ad
Source noteuspto-grants-2015_09