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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 523447Generated: October 29, 2026

Water → HCID 86732660, compound

https://huagongshe.com/reaction/523447

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantN-bromobutanimideHCID 67184—
Reactant5-Phenylphenanthridin-6(5H)-oneHCID 317989—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
ProductHCID 86732660HCID 86732660—

Reaction Steps

6.0 g (22 2 mmol) of 5-phenyl-5H-phenanthridin-6-one are initially introduced in 150 ml of CH2Cl2. A solution of 4 g (22 5 mmol) of NBS in 100 ml of acetonitrile is subsequently added dropwise at −15° C. with exclusion of light, 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: 7.4 g (21 mmol), 80% of theory, purity according to 1H-NMR about 96%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09337430B2
Source datasetuspto-grants-2016_05
ORD IDord-7d9655b9d04a46d7937d88da132e2347
Source noteuspto-grants-2016_05