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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1995495Erstellt: 24. Oktober 2026

Potassium Carbonate → 2-[(2-Chloro-6-fluorophenyl)methyl]-4,4-dimethyl-1,2-oxazolidin-3-one

https://huagongshe.com/de/reaction/1995495

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
Edukt1-Chloro-2-(chloromethyl)-3-fluorobenzeneHCID 108675—
Edukt4,4-Dimethyl-1,2-oxazolidin-3-oneHCID 642151—
Katalysator18-Crown-6HCID 28557—
LösungsmittelAcetonitrileHCID 6342—
Produkt2-[(2-Chloro-6-fluorophenyl)methyl]-4,4-dimethyl-1,2-oxazolidin-3-oneHCID 1319257146,6%

Reaktionsschritte

To a stirred suspension of 3.6 grams (0.026 mole) of potassium carbonate and 0.14 gram (0.0005 mole) of 1,4,7,10,13,16-hexaoxacyclooctadecane in 50 ml of acetonitrile was added dropwise a solution of 3.0 grams (0.026 mole) of 4,4-dimethyl-3-isoxazolidinone (Example 30, Step B) and 4.7 grams (0.025 mole) of (2-chloro-6-fluorophenyl)methyl chloride in 25 ml of acetonitrile. The complete addition required 30 minutes. Upon completion of addition the reaction mixture was stirred at ambient temperature for 18 hours, and then filtered. The filtrate was diluted with 200 ml of methylene chloride and washed with three 100-ml portions of water. The organic layer was dried with magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure to give an oil residue. The oil solidified and was recrystallized from petroleum ether to give 3.0 grams of 2-[(2-chloro-6-fluorophenyl)methyl]-4,4-dimethyl-3-isoxazolidinone; mp 49°-51°.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04405357
Quelldatensatzuspto-grants-1983_09
ORD IDord-1723d66cf886499e90e70065fbeed7c3
Quellennotizuspto-grants-1983_09