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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1513889Generated: October 26, 2026

2-Bromo-1,3,4-trifluorobenzene → [6-Methoxy-2-(2,3,6-trifluoro-phenyl)-naphthalen-1-yl]-[4-(2-piperidin-1-yl-ethoxy)-phenyl]-methanone

https://huagongshe.com/reaction/1513889

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-1,3,4-trifluorobenzeneHCID 2736401—
Reactant4-(2-(Piperidin-1-yl)ethoxy)benzaldehydeHCID 11183892—
ReactantTrifluoromethanesulfonic acid 6-methoxy-1-[4-(2-piperidin-1-yl-ethoxy)benzoyl]-naphthalen-2-yl esterHCID 11685250—
Product[6-Methoxy-2-(2,3,6-trifluoro-phenyl)-naphthalen-1-yl]-[4-(2-piperidin-1-yl-ethoxy)-phenyl]-methanoneHCID 5755252545.1%

Reaction Steps

Couple trifluoromethanesulfonic acid 6-methoxy-1-[4-(2-piperidin-1-yl-ethoxy)-benzoyl]-naphthalen-2-yl ester (1.81 g, 3.37 mmol) with 2-bromo-1,3,4-trifluoro-benzene (1.42 g, 6.75 mmol) in a procedure similar to the preparation of 6-hydroxy-2-(2,3,5-trifluoro-phenyl)-naphthalen-1-yl]-[4-(2-piperidin-1-yl-ethoxy)-phenyl]-methanone to give 0.79 g (45%) of the title compound: mass spectrum (ion spray) m/z=520.3 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08217032B2
Source datasetuspto-grants-2012_07
ORD IDord-c017a01e43ac4111abc3258396497b0b
Source noteuspto-grants-2012_07