HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 574248Generated: October 25, 2026
Triphenylphosphine → HCID 87285738, compound
https://huagongshe.com/reaction/574248
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | Carbamic acid, N-((1R)-2-hydroxy-1-phenylethyl)-, 1,1-dimethylethyl ester | HCID 7016461 | — |
| Reactant | 1-(2,6-difluoro-benzyl)-5-nitro-1H-pyrimidine-2,4-dione | HCID 24757354 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 87285738 | HCID 87285738 | 67% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09034850B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-ed4a59c3fa0f4e62a077c3689ed2d951 |
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| Source note | uspto-grants-2015_05 |
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