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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2410464Generated: October 26, 2026

Potassium Bromide → 3-(4'-Fluorobiphenyl-4-yl)propanal

https://huagongshe.com/reaction/2410464

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium BromideHCID 253877—
ReactantSodium BicarbonateHCID 516892—
Reactant[1,1'-Biphenyl]-4-propanoicacid, 4'-fluoro-HCID 1393679—
ReactantSodium HypochloriteHCID 23665760—
CatalystTempoHCID 2724126—
SolventDichloromethaneHCID 6344—
Product3-(4'-Fluorobiphenyl-4-yl)propanalHCID 86700983—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of the compound obtained from step d above (0.7 g) in dichloromethane (10 mL), 2,2,6,6-tetramethylpiperidine N-oxyl (4.74 mg) and potassium bromide (36.05 mg) were added at 0° C. under nitrogen atmosphere. Sodium hypochlorite (0.28 g, 4% solution) was added at pH 8-9 (maintained by adding aqueous sodium bicarbonate solution). The reaction mixture was stirred for 20 minutes at 0° C. The organic layer was separated and the aqueous layer was extracted with dichloromethane. The combined organic layers were washed with saturated aqueous sodium bicarbonate solution, water, and brine. The organic layer was dried over anhydrous sodium sulphate, filtered, and concentrated under reduced pressure to afford the title compound (0.55 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08816073B2
Source datasetuspto-grants-2014_08
ORD IDord-85f76d7940164c20bcfa6d8e2fab9beb
Source noteuspto-grants-2014_08