HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 735327Generated: October 30, 2026
Triphenylphosphine → HCID 68899028, compound
https://huagongshe.com/reaction/735327
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 57421915 | HCID 57421915 | — |
| Reactant | HCID 65416705 | HCID 65416705 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Hexamethylphosphoramide | HCID 12679 | — |
| Product | HCID 68899028 | HCID 68899028 | 10.2% |
Reaction Steps
1-(2,4-Difluorophenyl)prop-2-en-1-ol (Step 3, 260 mg, 1.41 mmol), [2-iodo-4-(phenylsulfonyl)phenyl]amine (Step 2, 359 mg, 1 mmol), palladium acetate (22 mg, 0.1 mmol), sodium hydrogencarbonate (162 mg, 3 mmol) and triphenylphosphine (26 mg, 0.1 mmol) were combined in hexamethylphosphoramide (5 mL) and heated to 140° C. for 16 hours. The reaction mixture was diluted with water and extracted with ethyl acetate. The combined organic layers were washed with brine (x5), dried over MgSO4 and evaporated. The residue was purified by preparative HPLC to give the title compound (39 mg). 1H NMR (500 MHz, CDCl3) δ 8.59 (1H, d), 8.32 (1H, d), 8.21-8.14 (2H, m), 8.10 (1H, dd, J=2.1, 8.9 Hz), 8.03-7.98 (3H, m), 7.61-7.52 (3H, m), 7.09-7.05 (1H, m), 6.99-6.94 (1H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07592456B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-3fdc9796593548c68e1eed9952289f3c |
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| Source note | uspto-grants-2009_09 |
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