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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2293848Generated: October 31, 2026

Acetic Acid → HCID 86749419, compound

https://huagongshe.com/reaction/2293848

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium BicarbonateHCID 516892—
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 86749420HCID 86749420—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86749419HCID 8674941988.3%

Reaction Steps

A solution of (S,E)-3-[[(1,1-Dimethylethyl)diphenylsilyl]oxy]-4-[[2-[4-(4-fluorophenyl)-2-(1-methylethyl)-6-phenyl-3-pyridinyl]ethenyl]methoxyphosphinyl]butanoic acid, methyl ester (826 mg, 1.10 mmol) in THF (10 ml) was treated with HOAc (320 ul, 336 mg, 5.6 mmol) and tetra-n-butylammonium fluoride (1.0M in THF, 3.3 ml, 3.3 mmol). After stirring at room temperature for 22 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, 30% acetone in hexane followed by 50% acetone in hexane). (S,E)-4-[[2-[4-(4-Fluorophenyl)-2-(1-methylethyl)-6-phenyl-3-pyridinyl]ethenyl]methoxyphosphinyl]-3-hydroxybutanoic acid, methyl ester (497 mg, 88%) was obtained as a white oily foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05686433
Source datasetuspto-grants-1997_11
ORD IDord-62107714d12b4b658a8c834dcd6a5925
Source noteuspto-grants-1997_11