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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2277345Generated: October 31, 2026

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

https://huagongshe.com/reaction/2277345

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 duced 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-089e765732e54b7db601251d4cac6374
Source noteuspto-grants-2015_09