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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1355673Generated: October 30, 2026

4-(Chloromethyl)pyridinium chloride → HCID 18507782, compound

https://huagongshe.com/reaction/1355673

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Chloromethyl)pyridinium chlorideHCID 74570—
ReactantHCID 18507786HCID 18507786—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18507782HCID 18507782—

Reaction Steps

To a solution of 6-bromo-7-methyl-1-naphthalen-2-ylmethyl-1,3-dihydro-indol-2-one (495.7 mg, 1.36 mmol) in THF (30 ml) was added 4-picolyl chloride hydrochloride (893 mg, 5.45 mmol). The resulting suspension was purged with nitrogen gas for 10 minutes, after which time an aqueous potassium hydroxide (1N, 10.88 ml, degassed for 10 minutes prior to the addition) was added dropwise at room temperature. The dark solution was stirred at room temperature overnight. After removal of THF, the reaction mixture was partitioned between water and ethyl ether. The organic layer was dried over MgSO4, filtered and concentrated under vacuum to give the crude product. It was chromatographed on flash silica gel eluting with ethyl acetate to provide the title compound of 2D (524 mg, 0.956 mmol, 70.3% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06586447B1
Source datasetuspto-grants-2003_07
ORD IDord-c9a3eac64cdd4824ad478e76cbcd68b1
Source noteuspto-grants-2003_07