Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 351574Generated: October 30, 2026

1,3,4,5-Tetrahydro-2H-1-benzazepin-2-one → 2,3,4,5-tetrahydro-1H-1-benzazepine

https://huagongshe.com/reaction/351574

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3,4,5-Tetrahydro-2H-1-benzazepin-2-oneHCID 248580—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Product2,3,4,5-tetrahydro-1H-1-benzazepineHCID 57650385%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 1,3,4,5-tetrahydrobenzo[b]azepin-2-one (12.9 g, 80.0 mmol) in 720 mL of tetrahydrofuran was added 80 mL of lithium aluminum hydride (1 M solution in tetrahydrofuran). The reaction mixture was stirred at reflux for 3 hours and cooled to 0° C. The reaction was quenched by the sequential addition of 3 mL of water, 3 mL of 15% sodium hydroxide, and 9 mL of water. The mixture was filtered through Celite and the filter cake rinsed with ethyl acetate. The filtrate was concentrated under reduced pressure to provide 10.0 g (85%) of the desired compound as an orange solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06743785B2
Source datasetuspto-grants-2004_06
ORD IDord-4064ede10cac43df8ca4a0121de7a409
Source noteuspto-grants-2004_06