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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 77989Generated: October 28, 2026

Diethyl Ether → HCID 59255292, compound

https://huagongshe.com/reaction/77989

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantDimethylformamideHCID 6228—
Reactant5-Bromo-2-(3-fluorophenoxy)pyridineHCID 59255220—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
ProductHCID 59255292HCID 5925529252%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a diethyl ether (100 mL) solution of 5-bromo-2-(3-fluoro-phenoxy)-pyridine (5.81 g, 21.7 mmol) described in Manufacturing Example 71-1-1 was added n-butyl lithium (13.8 mL, 1.57 M n-hexane solution, 21.7 mmol) under nitrogen atmosphere at −78° C., which was stirred for 40 minutes at −78° C. N,N-Dimethylformamide (2.02 mL, 26.0 mmol) was then added to the mixture at −78° C., and stirred for 25 minutes as the temperature was gradually raised to 0° C. Water was added to the reaction solution at 0° C., which was then extracted with ethyl acetate. The organic layer was separated, washed with 1 N aqueous sodium hydroxide solution and saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, and filtered. The filtrate was concentrated under a reduced pressure, and the residue was purified by silica gel column chromatography (heptane:ethyl acetate=5:1) to obtain the title compound (2.47 g, 52%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841327B2
Source datasetuspto-grants-2014_09
ORD IDord-21c8bed34e464c4caa8d10eb1d1ba7fd
Source noteuspto-grants-2014_09