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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 574248Generated: October 25, 2026

Triphenylphosphine → HCID 87285738, compound

https://huagongshe.com/reaction/574248

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
ReactantCarbamic acid, N-((1R)-2-hydroxy-1-phenylethyl)-, 1,1-dimethylethyl esterHCID 7016461—
Reactant1-(2,6-difluoro-benzyl)-5-nitro-1H-pyrimidine-2,4-dioneHCID 24757354—
SolventTetrahydrofuranHCID 8028—
ProductHCID 87285738HCID 8728573867%

Reaction Steps

1-(2,6-difluoro-benzyl)-5-nitro-1H-pyrimidine-2,4-dione (82 mg, 0.29 mmol), ((R)-2-hydroxy-1-phenyl-ethyl)-carbamic acid tert-butyl ester (69 mg, 0.29 mmol), and triphenylphosphine (114 mg, 0.44 mmol) were dissolved in anhydrous tetrahydrofuran (2 mL). To this solution was added diethyl azodicarboxylate (200 μl, 0.44 mmol), followed by stirring at room temperature for 4 hrs. The solution was concentrated, after which the residue was purified using silica gel chromatography (eluent: hexane/ethyl acetate/dichloromethane, 3/1/1) and dried in a vacuum to afford 67 mg of the compound as a colorless oil (yield 67%). 1H NMR (300 MHz, CDCl3) δ 1.30 (9H, s), 3.40 (1H, d), 4.50 (1H, m), 5.08-5.27 (4H, m), 7.02 (2H, t), 7.26-7.47 (6H, m), 8.78 (1H, s)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09034850B2
Source datasetuspto-grants-2015_05
ORD IDord-ed4a59c3fa0f4e62a077c3689ed2d951
Source noteuspto-grants-2015_05