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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1757354Generated: October 26, 2026

1-Bromooctane → HCID 19387529, compound

https://huagongshe.com/reaction/1757354

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BromooctaneHCID 8140—
ReactantMagnesiumHCID 5462224—
Reactant5-Bromo-3-fluoro-2-(4-octyloxyphenyl)pyridineHCID 19387546—
CatalystHCID 178418745HCID 178418745—
SolventTetrahydrofuranHCID 8028—
ProductHCID 19387529HCID 1938752981.7%

Reaction Conditions

Temperature-10 °C

Reaction Steps

0.30 g (12.30 mmol) of magnesium and 2.16 g (11.18 mmol) of octyl bromide in 10 ml of tetrahydrofuran are used to prepare, at 50° C. for 2 hours, the solution of the Grignard compound, which is added dropwise to a solution, cooled to -10° C. of 2.13 g (5.59 mmol) of 5-bromo-3-fluoro-2-(4-octyloxyphenyl)pyridine and 0.03 g (0.06 mmol) of [1,3-bis(diphenylphosphino)propane]nickel(II) chloride in 60 ml of tetrahydrofuran, and the mixture is stirred at -10° C. for 3 hours. The mixture is subsequently partitioned between ether and aqueous ammonium chloride solution, and the organic phase is washed twice with aqueous sodium chloride solution, dried over sodium sulfate and evaporated to dryness. Chromatographic purification (silica gel/dichloromethane:hexane 7:3) gives 1.89 g of 3-fluoro-5-octyl-2-(4-octyloxyphenyl)pyridine. ##STR16## The compound has the phase sequence: X 25.5 (5) N 35 I.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05445763
Source datasetuspto-grants-1995_08
ORD IDord-1464881ae1654787abf1fbdb162a51cf
Source noteuspto-grants-1995_08