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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1954922Generated: November 1, 2026

Butyryl chloride → 4'-Fluorobutyrophenone

https://huagongshe.com/reaction/1954922

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyryl chlorideHCID 8855—
ReactantFluorobenzeneHCID 10008—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventDichloromethaneHCID 6344—
Product4'-FluorobutyrophenoneHCID 6849880.2%

Reaction Conditions

Temperature25 °C

Reaction Steps

Aluminum chloride (1.39 g, 1.04 mol) was added to a solution of butyryl chloride (55.45 g, 0.520 mol, Aldrich) in dichloromethane (500 ml) stirring under a nitrogen atmosphere at 25° C. A solution of fluorobenzene (50.1 g, 0.521 mol, Aldrich) in dichloromethane was added and stirring was continued for 18 h. The reaction solution was poured over ice and extracted with dichloromethane (3×400 ml). The combined dichloromethane extractions were washed with deionized water (2×250 ml), 1.0N hydrochloric acid (500 ml), saturated sodium bicarbonate solution (2×500 ml) and deionized water (4×250 ml), concentrated by spin evaporation in vacuo. This material was combined with material from a similar preparation (using 0.26 mol of fluorobenzene) for distillation. Distillation at reduced pressure gave 69.27 g (53%) of 4'-fluorobutyrophenone as a pale yellow liquid which later partially crystallized, b.p. 108-112° C. at 30 millitorr: NMR (DMSO-d6): d 8.03 (q, 2H, J=9.0 Hz and 5.6 Hz), 7.31 (t, 2H, J=8.9 Hz), 2.97 (t, 2H, J=7.0 Hz), 1.65-1.55 (m, 2H), 0.91 (t, 3H, J=7.3 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06124284
Source datasetuspto-grants-2000_09
ORD IDord-683ec53c43264f14bdb654ed5db40adf
Source noteuspto-grants-2000_09