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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 25168Generated: October 30, 2026

p-Toluenesulfonic acid → 1,5,6,7-tetrahydro-1-(4-bromophenyl]-3-(morpholin-4-yl)-2H-azepin-2-one

https://huagongshe.com/reaction/25168

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantMorpholineHCID 8083—
ReactantHCID 22566235HCID 22566235—
SolventBenzeneHCID 241—
Product1,5,6,7-tetrahydro-1-(4-bromophenyl]-3-(morpholin-4-yl)-2H-azepin-2-oneHCID 22566255—

Reaction Steps

N-[4-bromophenyl]-3-oxocaprolactam (1.31 g, 4.63 mmol), morpholine (1.60 mL, 18.52 mmol), and p-toluenesulfonic acid (catalytic amount) were refluxed with 50 mL benzene using a Dean Stark apparatus under N2 for 12 h. The solvent was then removed in vacuo and the residue was dried under vacuum to give 1,5,6,7-tetrahydro-1-[4-bromophenyl]-3-(morpholin-4-yl)-2H-azepin-2-one as a yellow solid. LRMS (AP+): 351.0, 353.0, (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06858616B2
Source datasetuspto-grants-2005_02
ORD IDord-665a33cc989d486aa027c615fc2cbc05
Source noteuspto-grants-2005_02