HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1995045Generated: October 30, 2026
2-[5-(4-Fluorophenoxy)-2-nitrophenoxy]propanoyl chloride → HCID 20441147, compound
https://huagongshe.com/reaction/1995045
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-[5-(4-Fluorophenoxy)-2-nitrophenoxy]propanoyl chloride | HCID 20441163 | — |
| Reactant | HCID 20441179 | HCID 20441179 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 20441147 | HCID 20441147 | — |
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
| 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-3c3571a462f14ef9ad3de8fee69547ac |
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| Source note | uspto-grants-1983_09 |
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