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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1873768Generated: November 1, 2026

Ethanol → 2-(4-Fluorophenyl)pyrimidine-5-carbaldehyde

https://huagongshe.com/reaction/1873768

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant4-Fluorobenzamidine HydrochlorideHCID 12456160—
ReactantPotassium tert-butoxideHCID 23665647—
Product2-(4-Fluorophenyl)pyrimidine-5-carbaldehydeHCID 14008472—

Reaction Steps

2 g (11.45 mmol) of 4-fluorobenzamidine hydrochloride, 4.09 g (11.45 mmol) of 2-dimethylaminomethylene-1,3-bis(dimethylimmonio)propane-bis(tetrafluoroborate) and 3.86 g (34.36 mmol) of potassium tert-butylate in 70 ml of ethanol were heated under reflux for 8 h. After concentration, water and ethyl acetate were added. The organic phase was washed with a potassium hydrogensulfate solution and water, dried and evaporated. Yield: 1.87 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304438B2
Source datasetuspto-grants-2012_11
ORD IDord-47cf127e15fa4ed292425bcae8ddc936
Source noteuspto-grants-2012_11