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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1035156Generated: October 31, 2026

Boron tribromide → N-Trifluoroacetyl-7-hydroxy-1-methyl-2,3,4,5-tetrahydro-1H-3benzazepine

https://huagongshe.com/reaction/1035156

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
ReactantHCID 22292800HCID 22292800—
SolventDichloromethaneHCID 6344—
ProductN-Trifluoroacetyl-7-hydroxy-1-methyl-2,3,4,5-tetrahydro-1H-3benzazepineHCID 2229279095.6%

Reaction Conditions

Temperature20 °C

Reaction Steps

A solution of N-trifluoroacetyl-7-methoxy-1-methyl-2,3,4,5-tetrahydro-1H-3-benzazepine (0.506 g, 1.76 mmol) in dichloromethane (20 mL) was treated with BBr3 (4.1 mL of a 1.0M solution in CH2Cl2, 4.1 mmol) and stirred overnight while warming to 20° C. The excess BBr3 was quenched with water, and the resulting mixture was diluted with ether (200 mL), washed with Na2CO3 (100 mL) and brine (100 mL), dried with Na2SO4 and concentrated. Flash chromatography (15% EtOAc in hexane, silica) resulted in 0.460 g of a white solid foam. MS calculated for C13H14F3NO2+H: 274, observed: 274.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546378B2
Source datasetuspto-grants-2013_10
ORD IDord-d5a3d6b42ece4e24a3cc9b13bdb3a184
Source noteuspto-grants-2013_10