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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1579150Generated: November 2, 2026

N-bromobutanimide → HCID 12813977, compound

https://huagongshe.com/reaction/1579150

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant5,11-dihydro-5-methyl-10H-dibenz[b,f]azepin-10-oneHCID 78620—
SolventDimethylformamideHCID 6228—
ProductHCID 12813977HCID 12813977100.5%

Reaction Steps

22.81 g of N-bromosuccimide were added over 15 minutes at room temperature to a solution of 25 g of 5-methyl-10,11-dihydro [5H] dibenzo (b,f) azepine-10-one in 250 ml of dimethylformamide under a nitrogen atmosphere and the mixture was stirred for 30 minutes at room temperature. The reaction mixture was poured into 2 liters of ice water and was extracted with ether. The ether extracts were washed with water, dried over magnesium sulfate and evaporated to dryness to obtain 34 g of 2-bromo-5-methyl-10,11-dihydro [5H] dibenzo (b,f) azepine-11-one. The product was dissolved in 100 ml of refluxing ethyl acetate and the solution was filtered hot and concentrated to the start of crystallization. The mixture was iced for 30 minutes and vacuum filtered. The recovered precipitate was washed with ethyl acetate and dried under reduced pressure to obtain 29.5 g of the said product in the form of pale yellow crystals melting at 128°-129°C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03931151
Source datasetuspto-grants-1976_01
ORD IDord-802e3c954f5a474aa0b1f6ee4fa0b522
Source noteuspto-grants-1976_01