HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1995041Generated: October 30, 2026
HCID 20441146, compound → HCID 20441150, compound
https://huagongshe.com/reaction/1995041
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 20441146 | HCID 20441146 | — |
| Reactant | HCID 20441173 | HCID 20441173 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 20441150 | HCID 20441150 | — |
Reaction Steps
N-Ethyl-N-(4,5-dimethyl-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-nitro-4-bromophenoxy)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-ethyl-N-(4,5-dimethyl-1,3-dioxolan-2-ylmethyl)-2-[2-nitro-5-(2-nitro-4-bromophenoxy)phenoxy]propionamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04402729 |
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| Source dataset | uspto-grants-1983_09 |
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| ORD ID | ord-27148893a298482689944740a196121a |
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| Source note | uspto-grants-1983_09 |
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