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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1946615Generated: October 26, 2026

Dibenz(b,f)azepine → (Z)-2-(5H-dibenzo[b,f]azepin-5-yl)acetonitrile

https://huagongshe.com/reaction/1946615

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDibenz(b,f)azepineHCID 9212—
ReactantBromoacetonitrileHCID 11534—
ReactantSodium HydroxideHCID 14798—
ReactantBis(tetrabutylammonium) sulphateHCID 11433187—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product(Z)-2-(5H-dibenzo[b,f]azepin-5-yl)acetonitrileHCID 1134529451.7%

Reaction Steps

(Z)-5H-dibenzo[b,f]azepine (0.1 g, 0.5 mmol), tetrabutylammonium sulfate (0.35 g, 1.0 mmol), 2-bromoacetonitrile (0.4 mL, 5.0 mmol) and 50% aqueous sodium hydroxide (1 mL) were mixed in DCM (1 mL) and the reaction mixture was stirred for 5 days. The mixture was diluted in water and the aqueous layer was extracted with DCM (2 times). The combined organic layers were dried over sodium sulfate, filtered and concentrated. The crude product was purified by flash chromatography (0% to 50% ethyl acetate in hexanes) to afford title compound 365 (60 mg, 50%). 1H NMR (CDCl3) δ (ppm): 7.36-7.31 (m, 2H), 7.26-7.23 (m, 2H), 7.17-7.11 (m, 4H), 6.76 (s, 2H), 4.47 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399452B2
Source datasetuspto-grants-2013_03
ORD IDord-c7d5b70a48ac4dff9ba305b165af43f1
Source noteuspto-grants-2013_03