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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1934787Generated: October 31, 2026

Water → 10,11-Dihydro-10-hydroxy-5H-dibenz[b,f]azepine-5-carbonitrile

https://huagongshe.com/reaction/1934787

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantN-bromobutanimideHCID 67184—
Reactant10,11-Dihydro-5H-dibenzo[b,f]azepine-5-carbonitrileHCID 11160338—
SolventDichloromethaneHCID 6344—
Product10,11-Dihydro-10-hydroxy-5H-dibenz[b,f]azepine-5-carbonitrileHCID 994277361%

Reaction Conditions

Temperature45 °C

Reaction Steps

13.2 g (0.060 mols) of (I) are dissolved at room temperature in 80 ml of CH2Cl2 under stirring, then 11.8 g (0.066 mols) of N-bromosuccinimide of purity above 98% and 0.70 g (0.003 mols) of di-tert-butyl-peroxalate are added under stirring. The reaction mixture is subjected to mild nitrogen stream for 5 minutes, then heated to 45° C. and stirred at this temperature for 85 minutes. The resulting suspension is added with 100 ml of demineralized water and 3 grams of polyethylene glycol with average molecular weight 400, then refluxed for 5 hours under strong stirring. After decanting at 30° C., the organic phase is separated, dried over 4 g of Na2SO4, filtered and the resulting solution is concentrated to 20 ml, added with 10 ml of hexane, cooled to 0-5° C. for 2 hours and filtered to obtain 8.64 g (61%) of (VI), m.p. 110-112° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06384217B1
Source datasetuspto-grants-2002_05
ORD IDord-7b11128e608e46afb61471f705308dd8
Source noteuspto-grants-2002_05