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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2358230Generated: November 2, 2026

Acetic acid, 2-(triphenylphosphoranylidene)-, ethyl ester → HCID 72459876, compound

https://huagongshe.com/reaction/2358230

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic acid, 2-(triphenylphosphoranylidene)-, ethyl esterHCID 70670—
ReactantHCID 58911255HCID 58911255—
SolventTetrahydrofuranHCID 8028—
ProductHCID 72459876HCID 72459876—

Reaction Conditions

Temperature0 °C

Reaction Steps

In a 0.3 1 three necked flask fitted with a magnetical stirrer and dropping funnel under inert atmosphere, 6.62 g (20.8 mmol, 1 eq) of 6-bromo-2,4-difluoro-3-(pyrrolidin-1-ylazo)-benzaldehyde a9 are dissolved in THF (100 ml) and cooled down to 0° C. Ethyl (triphenylphosphoranylidene)acetate (9.43 g, 1.3 eq) is then added under efficient stirring, the temperature raising to 10° C. The mixture is kept under stirring one hour at 0° C., and then overnight at room temperature. The mixture is concentrated to dryness, the residue suspended in diethyl ether, the triphenylphospine oxide is filtered off and the filtrate concentrated to dryness. The residue is purified by PrepLC on silicagel (CH2Cl2/pentane: 50/50 (v/v)) to give 4.17 g of pure of 3-[6-bromo-2,4-difluoro-3-(pyrrolidin-1-ylazo)-phenyl]-acrylic acid ethyl ester a10 (47%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07763644B2
Source datasetuspto-grants-2010_07
ORD IDord-ee6538bb2ceb4f41a8008134bc97c825
Source noteuspto-grants-2010_07