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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1995044Generated: October 30, 2026

1-(1,3-Dioxolan-2-yl)methanamine → N-(1,3-dioxolan-2-ylmethyl)-2-[2-nitro-5-(2-chloro-4-trifluoromethylphenoxy)phenoxy]butyramide

https://huagongshe.com/reaction/1995044

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(1,3-Dioxolan-2-yl)methanamineHCID 10855394—
ReactantHCID 20441129HCID 20441129—
SolventDichloromethaneHCID 6344—
ProductN-(1,3-dioxolan-2-ylmethyl)-2-[2-nitro-5-(2-chloro-4-trifluoromethylphenoxy)phenoxy]butyramideHCID 20441174—

Reaction Conditions

Temperature-15 °C

Reaction Steps

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

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04402729
Source datasetuspto-grants-1983_09
ORD IDord-6d30d0b1563044c492d355d7f59049a9
Source noteuspto-grants-1983_09