Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1485586Generated: October 31, 2026

Water → 6-Bromo-1-fluoro-9-(2-nitrophenyl)-9H-carbazole

https://huagongshe.com/reaction/1485586

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantN-bromobutanimideHCID 67184—
Reactantfluoro-9-(2-nitrophenyl)-9H-carbazoleHCID 67324830—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
Product6-Bromo-1-fluoro-9-(2-nitrophenyl)-9H-carbazoleHCID 67325347—

Reaction Steps

6.7 g (22.2 mmol) of fluoro-9-(2-nitrophenyl]-9H-carbazole 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 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 the solid is isolated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09422287B2
Source datasetuspto-grants-2016_08
ORD IDord-d01b95dd9dd44c08972351726144fff7
Source noteuspto-grants-2016_08