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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2295223Generated: November 4, 2026

Acetic Acid → HCID 86749429, compound

https://huagongshe.com/reaction/2295223

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium BicarbonateHCID 516892—
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 86749430HCID 86749430—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86749429HCID 8674942978%

Reaction Steps

A solution of (S,E)-3-[[1,1-Dimethylethyl)-diphenylsilyl]oxy]-4-[[2-[2-(4-fluorophenyl)-4-(1-methylethyl)-6-phenyl-3-pyridinyl]ethenyl]-methoxyphosphinyl]butanoic acid, methyl ester (241 mg, 0.321 mmol) in THF (7 ml) was treated with HOAc (92 ul, 96 mg, 1.61 mmol) and tetra-n-butylammonium fluoride (1.0M in THF, 963 ul, 0.963 mmol). After stirring at room temperature for 18 hours, the solution was poured into saturated NaHCO3 and extracted with EtOAc. The EtOAc extract was washed with brine, dried, (Na2 SO4), filtered, and stripped to give an oil which was subsequently chromatographed (flash, Merck SiO2, 1:1 acetone:hexane followed 100% acetone). (S,E)-4-[[2-[2-(4-Fluorophenyl)-4-(1-methylethyl)-6-phenyl-3-pyridinyl]ethenyl]-methoxyphosphinyl]butanoic acid, methyl ester (124 mg, 76%) was obtained as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05691322
Source datasetuspto-grants-1997_11
ORD IDord-ca73e4ae1f5c43a09b04aaf74f5d22a5
Source noteuspto-grants-1997_11