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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 735327Generated: October 30, 2026

Triphenylphosphine → HCID 68899028, compound

https://huagongshe.com/reaction/735327

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 57421915HCID 57421915—
ReactantHCID 65416705HCID 65416705—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventHexamethylphosphoramideHCID 12679—
ProductHCID 68899028HCID 6889902810.2%

Reaction Conditions

Temperature140 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07592456B2
Source datasetuspto-grants-2009_09
ORD IDord-3fdc9796593548c68e1eed9952289f3c
Source noteuspto-grants-2009_09