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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 967264Generated: October 30, 2026

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

https://huagongshe.com/reaction/967264

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 numberUS06953787B2
Source datasetuspto-grants-2005_10
ORD IDord-84e02e09f1174bea9868495f0f7f4667
Source noteuspto-grants-2005_10