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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1632912Generated: November 2, 2026

2-[5-(4-Fluorophenoxy)-2-nitrophenoxy]propanoyl chloride → HCID 20441147, compound

https://huagongshe.com/reaction/1632912

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-[5-(4-Fluorophenoxy)-2-nitrophenoxy]propanoyl chlorideHCID 20441163—
ReactantHCID 20441179HCID 20441179—
SolventDichloromethaneHCID 6344—
ProductHCID 20441147HCID 20441147—

Reaction Conditions

Temperature-15 °C

Reaction Steps

N-(4-Bromo-1,3-dioxan-2-ylmethyl)amine (0.015 mole) triethylamine (5 ml) and methylene chloride (50 ml) are charged into a glass reaction vessel equipped with a mechanical stirrer, thermometer and addition funnel. The reaction mixture is cooled to about -15° C. and a solution of 2-[2-nitro-5-(4-fluorophenoxy)phenoxy]propionyl chloride (0.01 mole) in methylene chloride (50 ml) is added dropwise with stirring. After the addition is completed the reaction mixture is allowed to warm to room temperature with continued stirring. After this time the mixture is transferred to a separatory funnel and is washed with water and dilute aqueous sodium bicarbonate. The washed solution is then dried, filtered and stripped of solvent leaving a residue. The residue is then recrystallized from a toluene/hexane mixture to yield the desired product N-(4-bromo-1,3-dioxan-2-ylmethyl)-2-[2-nitro-5-(4-fluorophenoxy)phenoxy]propionamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04478634
Source datasetuspto-grants-1984_10
ORD IDord-5fe8c3515f414946889867d9fd114e33
Source noteuspto-grants-1984_10