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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1885659Generated: October 25, 2026

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

https://huagongshe.com/reaction/1885659

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantFluorobenzeneHCID 10008—
ReactantOctanedioyl dichlorideHCID 534653—
ReactantAluminum(III) ChlorideHCID 6451240—
Product1,8-Bis(4-fluorophenyl)octane-1,8-dioneHCID 188474767.3%

Reaction Steps

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%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05145937
Source datasetuspto-grants-1992_09
ORD IDord-cbbcfbf5ccb0474c9c1ec92e26b65d97
Source noteuspto-grants-1992_09