Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1421910Generated: October 30, 2026

4-(Chloromethyl)pyridine → 3-(Benzhydrylidene-amino)-3-pyridin-4-ylmethyl-dihydro-furan-2-one

https://huagongshe.com/reaction/1421910

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Chloromethyl)pyridineHCID 74571—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
Reactant3-[(diphenylmethylene)amino]dihydrofuran-2(3H)-oneHCID 13230916—
SolventTetrahydrofuranHCID 8028—
Product3-(Benzhydrylidene-amino)-3-pyridin-4-ylmethyl-dihydro-furan-2-oneHCID 5413902449.9%

Reaction Conditions

Temperature-40 °C

Reaction Steps

Potassium bis-(trimethylsilyl)amide (2.67, 13.4 mMol) was dissolved in anhydrous THF (50 mL) under an atmosphere of dry N2. The mixture was cooled to -40° C. to which was added a solution of 3-(benzhydrylidene-amino)-dihydro-furan-2-one (3.38 g, 12.7 mMol) in THF (30 mL). The mixture was warmed to ambient temperature and stirred at this temperature for 30 minutes. The solution was then cooled to -40° C. and a solution of 4-picolyl chloride (1.70 g, 13.4 mMol) in THF (20 mL) was added. The reaction mixture was warmed to ambient temperature and stirred for 18 hours. The mixture was partitioned between ethyl acetate-(EtOAc) and water. The organic layer was dried over sodium sulfate (Na2SO4), filtered and concentrated under vacuum to give a yellow oil. The oil was chromatographed on flash silica gel eluting with a gradient of EtOAc-hexanes (50:50) to EtOAc-hexanes (60:40 ) to give 2.26 g of the titled compound as an oil which crystallizes to a white solid upon standing.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06080769
Source datasetuspto-grants-2000_06
ORD IDord-6ed05d495d274515b80b41c738812580
Source noteuspto-grants-2000_06