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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 349741Erstellt: 24. Oktober 2026

1,2-Dichloro-4-fluorobenzene → HCID 11212544, Verbindung

https://huagongshe.com/de/reaction/349741

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,2-Dichloro-4-fluorobenzeneHCID 74028—
EduktSodium BicarbonateHCID 516892—
Edukttert-Butyl 4-hydroxy-[1,4'-bipiperidine]-1'-carboxylateHCID 9835508—
EduktPotassium tert-butoxideHCID 23665647—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 11212544HCID 11212544—

Reaktionsschritte

To a solution of potassium tert-butoxide (139.0 g, 1.24 mol) in THF (500 ml) was added a solution of the product of Step 1 (176.2 g, 0.62 mol) in THF (1000 ml). The reaction mixture was stirred 10 minutes before the additon of 3,4 dichlorofluorobenzene (122.8 g, 0.74 mol), this caused a green colouration that subsequently faded. The reaction mixture was then heated at reflux for 90 minutes. The reaction mixture was then cooled to room temperature before the addition of saturated NaHCO3 (1600 ml). The layers were separated and the organic layer stripped to leave an orange semi-solid. The solid was dissolved in DCM (1500 ml) and dried (MgSO4), filtered and the solvent removed. To the resultant solid was added methyl tert-butyl ether (MTBE) (54 ml) and iso-hexane (1000 ml) to give a slurry which was stirred overnight. The slurry was then filtered and washed with isohexane (200 ml) and the solid dried in vacuo at 50° C. to give the sub-titled compound as a pale powder, (211.6 g, 80%; MS: (M+H) 429).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07179922B2
Quelldatensatzuspto-grants-2007_02
ORD IDord-fa76b7452d9a43bf95ccd356985efa47
Quellennotizuspto-grants-2007_02