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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1650867Generated: October 30, 2026

Phosphoric Acid → HCID 15056094, compound

https://huagongshe.com/reaction/1650867

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphoric AcidHCID 1004—
ReactantTriphenylphosphineHCID 11776—
ReactantSodium 2-ethylhexanoateHCID 23672331—
ReactantHCID 86743934HCID 86743934—
ReactantHCID 178418361HCID 178418361—
CatalystPalladium hydroxideHCID 9942167—
CatalystHCID 178418397HCID 178418397—
SolventTetrahydrofuranHCID 8028—
ProductHCID 15056094HCID 1505609442.1%

Reaction Steps

To a solution of allyl (4R,5S,6S)-6-[(1R)-1-hydroxyethyl]-3-[(2S,4S)-2-(2,5-dioxoimidazolidin-1-yl)methyl-1-(4-nitrobenzyloxycarbonyl)pyrrolidin-4-yl]thio-4-methyl-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate (1.44 g) in tetrahydrofuran (30 ml) were added triphenylphosphine (0.29 g), sodium 2-ethylhexanoate (0.41 g) and tetrakis(triphenylphosphine)palladium(0) (0.13 g) successively with stirring at ambient temperature After stirring at the same temperature for 1 hour, the reaction mixture was evaporated in vacuo to give a residue. A mixture of the residue, 20% palladium hydroxide on carbon (0.5 g), 0.1M phosphoric acid buffer (pH 5.8,60 ml) and tetrahydrofuran (60 ml) was stirred for 5 hours under atmospheric pressure of hydrogen at ambient temperature. After the catalyst was filtered off, the filtrate was evaporated in vacuo to remove the organic solvent. The residue was chromatographed on nonionic adsorption resin, "Diaion HP-20" (Trademark, made by Mitsubishi Chemical Industries)(30 ml) eluting in turn with water (80 ml) and 5% aqueous acetone (90 ml). The fractions containing the desired compound were collected and lyophilized to give (4R,5S,6S)-6-[(1R)-1-hydroxyethyl]-3-[(2S,4S)-2-(2,5-dioxoimidazolidin-1-yl)methylpyrrolidin-4-yl]thio-4-methyl-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid (0.40 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04925838
Source datasetuspto-grants-1990_05
ORD IDord-f41b3a05c4914f57b039f35332a00b65
Source noteuspto-grants-1990_05