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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1689714Generated: October 30, 2026

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

https://huagongshe.com/reaction/1689714

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 numberUS08153621B2
Source datasetuspto-grants-2012_04
ORD IDord-9be2b57d54fa466a8bc13d0d13345576
Source noteuspto-grants-2012_04