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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1035357Generated: October 31, 2026

N-bromobutanimide → N-trifluoroacetyl-8-bromo-1-ethyl-7-methoxy-2,3,4,5tetrahydro-1H-3-benzazepine

https://huagongshe.com/reaction/1035357

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 22292778HCID 22292778—
SolventAcetonitrileHCID 6342—
ProductN-trifluoroacetyl-8-bromo-1-ethyl-7-methoxy-2,3,4,5tetrahydro-1H-3-benzazepineHCID 2229282462.5%

Reaction Steps

A solution of N-trifluoroacetyl-1-ethyl-7-methoxy-2,3,4,5-tetrahydro-1H-3-benzazepine (0.710 g, 2.36 mmol) in acetonitrile (20 mL) was treated with N-bromosuccinimide (0.504 g, 2.83 mmol), and stirred overnight at 20 C. The product mixture was concentrated, diluted with EtOAc (100 mL), washed with water (50 mL) and brine (50 mL), dried with Na2SO4 and concentrated. Flash chromatography (10% EtOAc in hexanes, silica) resulted in 0.561 g of a clear oil. MS calculated for C15H17BrF3NO2+H: 380, observed: 380.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546379B2
Source datasetuspto-grants-2013_10
ORD IDord-97f6297217804b27883514fcfa96c3cb
Source noteuspto-grants-2013_10