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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1689682Generated: October 29, 2026

Boron tribromide → N-Trifluoroacetyl-7-hydroxy-8-iodo-1-methyl-2,3,4,5-tetrahydro-1H-3-benzazepine

https://huagongshe.com/reaction/1689682

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
ReactantN-trifluoroacetyl-8-iodo-7-methoxy-1-methyl-2,3,4,5-tetrahydro-1H-3-benzazepineHCID 22292785—
SolventDichloromethaneHCID 6344—
ProductN-Trifluoroacetyl-7-hydroxy-8-iodo-1-methyl-2,3,4,5-tetrahydro-1H-3-benzazepineHCID 2229281597.6%

Reaction Conditions

Temperature20 °C

Reaction Steps

A solution of N-trifluoroacetyl-8-iodo-7-methoxy-1-methyl-2,3,4,5-tetrahydro-1H-3-benzazepine (80 mg, 0.19 mmol) in dichloromethane (3 mL) was treated with BBr3 (0.40 mL of a 1.0M solution in CH2Cl2, 0.40 mmol) and stirred overnight at 20° C. The excess BBr3 was quenched with water and the product mixture was diluted with ether (20 mL), washed with Na2CO3 (10 mL) and brine (10 mL), dried with Na2SO4 and concentrated. Flash chromatography (15% EtOAc in hexane, silica) resulted in 74 mg of a white solid. MS calculated for C13H13F3INO2+H: 400, observed: 400.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153621B2
Source datasetuspto-grants-2012_04
ORD IDord-73dba9325f4b440ab82f480c9c1ab44f
Source noteuspto-grants-2012_04