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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1035359Generated: October 30, 2026

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

https://huagongshe.com/reaction/1035359

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosuccinimideHCID 31398—
ReactantHCID 22292778HCID 22292778—
SolventAcetonitrileHCID 6342—
ProductN-trifluoroacetyl-8-chloro-1-ethyl-7-methoxy-2,3,4,5-tetrahydro-1H-3-benzazepineHCID 22292817391.8%

Reaction Steps

A solution of N-trifluoroacetyl-1-ethyl-7-methoxy-2,3,4,5-tetrahydro-1H-3-benzazepine (0.600 g, 1.99 mmol) in acetonitrile (20 mL) was treated with N-chlorosuccinimide (0.057 g, 0.32 mmol), and stirred overnight at 60 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 0.421 g of a clear oil. MS calculated for C15H17ClF3NO2+H: 336, observed: 336.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546379B2
Source datasetuspto-grants-2013_10
ORD IDord-abde761a6dc74f1ba433f8e9cfe5ffa2
Source noteuspto-grants-2013_10