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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 865922Generated: October 31, 2026

Dimethylformamide → HCID 15279439, compound

https://huagongshe.com/reaction/865922

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantLithium ChlorideHCID 433294—
Reactant2-(Tributylstannyl)pyridineHCID 607784—
Reactant2,2-Dimethyl-4-oxo-4H-benzo[D][1,3]dioxin-5-YL trifluoromethanesulfonateHCID 10892748—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 15279439HCID 15279439—

Reaction Steps

6.0 g (18.4 mmol) of 2,2-dimethyl-5-trifluoromethylsulfonyloxy-4H-(1,3)benzodioxin-4-one, 7.0 g (19.0 mmol) of 2-tributylstannylpyridine, 2.3 g (55.2 mmol) of lithium chloride and 420 mg (0.36 mmol) of tetrakistriphenylphosphinepalladium0 are dissolved in 60 ml of dioxane and 90 ml of dimethylformamide and the mixture is refluxed for 1.5 h (reaction temperature about 120° C.). It is stirred into 1.4 l of water at 0° C. and extracted with methyl tert-butyl ether, and the extract is washed with water and sodium chloride solution, dried over sodium sulfate and concentrated in vacuo. The residue is taken up in 60 ml of ethyl acetate, 8 g of potassium fluoride are added and the mixture is stirred overnight. The solid is filtered off and subsequently washed with plenty of ethyl acetate, and the filtrate is concentrated in vacuo. The crude product is purified by chromatography on silica gel 60 using hexane/ethyl acetate. Yield: 2.39 g (51%). Melting point: 142° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05569640
Source datasetuspto-grants-1996_10
ORD IDord-135520d35c4b446d9a6fd5d2e7dd6a7c
Source noteuspto-grants-1996_10