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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 235137Generated: October 25, 2026

Triethylamine → 7-(3-Fluorophenyl)-1-(4-methyl-1-piperazinyl)-naphthalene

https://huagongshe.com/reaction/235137

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-Bromo-3-fluorobenzeneHCID 14082—
ReactantLithium ChlorideHCID 433294—
Reactant7-Trimethylstannyl-1-(4-methyl-1-piperazinyl)-naphthaleneHCID 22115608—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
SolventDimethylformamideHCID 6228—
SolventDiethylether hexaneHCID 21584099—
Product7-(3-Fluorophenyl)-1-(4-methyl-1-piperazinyl)-naphthaleneHCID 18967542—

Reaction Steps

The title product was prepared following the procedure of example 41 from 7-trimethylstannyl-1-(4-methyl-1-piperazinyl)-naphthalene (0.25 g, 0.67 mmol), 3-fluoro-1-bromobenzene (0.13 g, 0.74 mmol), triethylamine (0.45 mL, 3.23 mmol), lithium chloride (0.088 g, 2.07 mmol), and bis (triphenylphosphine) palladium chloride (0.025 g, 0.036 mmol) in DMF (12.5 mL) with a heating time of 2 hours at 120 to 130° C. The product obtained was 0.13 g (59%) in yield. A sample was obtained by recrystallization from ether/hexane for analysis: mp 116°-116.5° C. Analysis calculated for C22H21FN2 : C, 79.49; H, 6.37; N, 8.43. Found: C, 79.07; H, 6.46; N, 8.66.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05597826
Source datasetuspto-grants-1997_01
ORD IDord-c707fa5df8a24a12a7bf570765c2d09d
Source noteuspto-grants-1997_01