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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1995043Generated: October 31, 2026

HCID 20441135, compound → HCID 20441145, compound

https://huagongshe.com/reaction/1995043

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 20441135HCID 20441135—
ReactantHCID 20441180HCID 20441180—
SolventDichloromethaneHCID 6344—
ProductHCID 20441145HCID 20441145—

Reaction Conditions

Temperature-15 °C

Reaction Steps

N-(4-Chloro-1,3-dioxolan-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-trifluoromethylphenoxy)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-chloro-1,3-dioxolan-2-ylmethyl)-2-[2-nitro-5-(4-trifluoromethylphenoxy)phenoxy]propionamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04402729
Source datasetuspto-grants-1983_09
ORD IDord-0833f31fd733477496472402916bd855
Source noteuspto-grants-1983_09