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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 13638Erstellt: 24. Oktober 2026

Sodium Chloride → 2-(2'-Bromo-4-fluorophenoxy)tetrahydro-2H-pyran

https://huagongshe.com/de/reaction/13638

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium ChlorideHCID 5234—
Edukt3,4-dihydro-2H-pyranHCID 8080—
EduktPotassium CarbonateHCID 11430—
EduktBenzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 466102—
Edukt2-Bromo-4-fluorophenolHCID 605472—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
Produkt2-(2'-Bromo-4-fluorophenoxy)tetrahydro-2H-pyranHCID 59340247—

Reaktionsschritte

A mixture of 478.0 ml (5.24 mol) of 3,4-dihydropyran and 750 ml of dichloromethane was admixed with 65.4 g (260 mmol) of pyridinium p-toluenesulfonate. Subsequently, a solution of 500.0 g (2.62 mmol) of 2-bromo-4-fluorophenol in 500 ml of dichloromethane was added dropwise. After stirring for 24 h, the reaction mixture was admixed with a solution of 50 g of potassium carbonate in 500 ml of water, and then with 500 ml of saturated sodium chloride solution. The organic phase was removed, dried over potassium carbonate and, after freeing it of the solvent and potassium carbonate, fractionally distilled (approx. 1 mbar, top temperature from 79 to 82° C.) by means of a Vigreux column (40 cm). The product was obtained as a colorless, low-viscosity oil. The yield was 520.5 g (72.2%) at a purity of greater than 98.0% by 1H NMR.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07728137B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-30441e9188ee410491001da6d20d30a7
Quellennotizuspto-grants-2010_06