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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 576744Generated: October 30, 2026

Triphenylphosphine → HCID 86723845, compound

https://huagongshe.com/reaction/576744

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
ReactantHCID 11483858HCID 11483858—
ReactantHCID 86723841HCID 86723841—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86723845HCID 8672384560.7%

Reaction Steps

To a solution of 1-(3-trifluoromethylphenyl)pyrimidin-2,4(1H,3H)-dione (prepared in Reference Example 98 or 99) (740.0 mg) in tetrahydrofuran (10.0 ml) was added (R)-1-(tert-butyldiphenylsilyloxy)propane-2-ol (1.82 g), triphenylphosphine (1.5 g) and diethyl azodicarboxylate (2.7 ml:2.2 M toluene solution) and the resulting mixture was stirred at room temperature for twelve hours. To the reaction mixture was added water (50 ml), and the resulting mixture was extracted with ethyl acetate (30 ml×2) and the organic layer was washed with water (20 ml) and saturated saline (20 ml), dried over anhydrous sodium sulfate and then concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: hexane/ethyl acetate) to afford (R)-3-[1-(tert-butyldiphenylsilyloxy)propane-2-yl]-1-(3-trifluoromethylphenyl)pyrimidin-2,4(1H,3H)-dione (969.8 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040516B2
Source datasetuspto-grants-2015_05
ORD IDord-88a3f28cf58847df881acbfb8a3450d0
Source noteuspto-grants-2015_05