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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1885659Erstellt: 26. Oktober 2026

Hydrochloric Acid → 1,8-Bis(4-fluorophenyl)octane-1,8-dione

https://huagongshe.com/reaction/1885659

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktFluorobenzeneHCID 10008—
EduktOctanedioyl dichlorideHCID 534653—
EduktAluminum(III) ChlorideHCID 6451240—
Produkt1,8-Bis(4-fluorophenyl)octane-1,8-dioneHCID 188474767,3%

Reaktionsschritte

Suberoyl chloride (40.8 g, 0.1933 mol) was added over a 30-45 minute period to a mechanically stirred suspension of aluminum chloride (64.4 g, 0.483 mol) in fluorobenzene (181 ml, 1.93 mol) maintained at 5°-10° C. The yellow slurry was allowed to warm to room temperature and was stirred overnight. The reaction mixture was poured onto approximately 1000 g of ice containing 75 ml of concentrated hydrochloric acid. The resulting suspension was separated by decantation and washed several times with water. The organic layer was distilled to remove excess fluorobenzene and the solid residue collected by filtration, washed with water, and dried at 100° C. The crude solid was recrystallized from approximately 500 ml of toluene to afford 43.0 g (67% yield) of 1,6-bis(4-fluorobenzoyl)hexane; mp 123°-124° C.; 'H NMR (CDCl3) δ1.0-2.1 (m, 8H, CH2), 2.97 (t, 4H, O=CCH2, J=7.0 Hz), 6.9-8.3 (m, 8H, aromatic). Anal. Calcd. for C20H20F2O2 : C, 72.71%; H, 6.10%; F, 11.50%. Found: C, 72.50%; H, 5.86%; F, 11.19%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05145937
Quelldatensatzuspto-grants-1992_09
ORD IDord-cbbcfbf5ccb0474c9c1ec92e26b65d97
Quellennotizuspto-grants-1992_09