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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2221838Generated: November 2, 2026

Dimethylformamide → HCID 86605801, compound

https://huagongshe.com/reaction/2221838

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantTetraethyl methylenediphosphonateHCID 15455—
ReactantSodium hydrideHCID 24758—
Reactant3-[4-[2-(2-furyl)-5-methyl-4-oxazolylmethoxy]-3-methoxybenzyloxy]-1-phenyl-1H-pyrazole-5-carbaldehydeHCID 86591671—
SolventWaterHCID 962—
ProductHCID 86605801HCID 8660580169%

Reaction Steps

To a mixture of 3-[(4-{[2-(2-furyl)-5-methyl-1,3-oxazol-4-yl]methoxy}-3-methoxybenzyl)oxy]-1-phenyl-1H-pyrazole-5-carbaldehyde (0.50 g), tetraethyl methylenediphosphonate (0.32 g) and N,N-dimethylformamide (10 mL) was added sodium hydride (60% in oil, 0.05 g) at room temperature, and the mixture was stirred at the same temperature for 1 hr. The reaction mixture was poured into water and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and concentrated. The residue was subjected to silica gel column chromatography to give diethyl (E)-2-{3-[(4-{[2-(2-furyl)-5-methyl-1,3-oxazol-4-yl]methoxy}-3-methoxybenzyl)oxy]-1-phenyl-1H-pyrazol-5-yl}ethenylphosphonate as a colorless oil (0.43 g, yield 69%) from a fraction eluted with ethyl acetate-hexane (3:1, v/v).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07368578B2
Source datasetuspto-grants-2008_05
ORD IDord-aed2dc5835bc430c9b2fb6a6a0f75875
Source noteuspto-grants-2008_05