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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 221235Generated: October 30, 2026

N-bromobutanimide → HCID 22292777, compound

https://huagongshe.com/reaction/221235

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 22292800HCID 22292800—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
ProductHCID 22292777HCID 2229277797.3%

Reaction Steps

A solution of N-trifluoroacetyl-7-methoxy-1-methyl-2,3,4,5-tetrahydro-1H-3-benzazepine (1.25 g, 4.35 mmol) in acetonitrile (40 mL) was treated with N-bromosuccinimide (0.852 g, 4.79 mmol) and stirred overnight at 20 C. The product mixture was diluted with EtOAc (200 mL), washed with saturated aqueous sodium bisulfite (100 mL) and brine (100 mL), dried with Na2SO4 and concentrated. Flash chromatography (15% EtOAc in hexane, silica) resulted in 1.55 g of a clear oil. 1H NMR (400 MHz, CDCl3, mixture of rotamers) d 7.34 (s, 1 H), 6.65 (m, 1 H), 3.87 (s, 3H), 3.81 (m, 1 H), 3.55 (m, 1.3 H), 3.37 (m, 0.7 H), 3.2-2.9 (bm, 4 H), 1.30 (m, 3 H). MS calculated for C14H15BrF3NO2+H: 366, observed: 366.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08207158B2
Source datasetuspto-grants-2012_06
ORD IDord-6005865fa69f419191410ce6d20b36b1
Source noteuspto-grants-2012_06