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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1672571Generated: October 30, 2026

Water → 4-(Pentafluoro-lambda6-sulfanyl)benzaldehyde

https://huagongshe.com/reaction/1672571

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantHexamethylphosphoramideHCID 12679—
Reactant4-Iodophenylsulfur PentafluorideHCID 2779199—
ReactantHCID 178418416HCID 178418416—
CatalystHCID 178418397HCID 178418397—
SolventAcetonitrileHCID 6342—
Product4-(Pentafluoro-lambda6-sulfanyl)benzaldehydeHCID 277920786%

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of 4-iodophenylsulfur pentafluoride (250 mg, 0.757 mmol) in acetonitrile (10 mL) was added to a 100 mL pressure bottle containing tetrakis(triphenylphosphine)palladium(0) (43.8 mg, 0.038 mmol), hexamethylphosphoramide (1.25 mL, 7.18 mmol), and poly(methylhydrosiloxane) (1.0 mL, 0.76 mmol). The reaction was pressurized with carbon monoxide (50 psi), and stirred for 20 hr at 80° C. The mixture was cooled to ambient temperature, water (100 mL) was added, and the product was extracted with Et2O (2×100 mL). The organic layer was washed with brine and dried over Na2SO4, filtered, and concentrated in vacuo to a yellow oil. The crude product was chromatographed on silica gel (Analogix® SF10-8G column, 0%-25% EtOAc/hexanes, 10 mL/min) to give 151 mg (86%) of the title compound as a colorless liquid. 1H NMR (300 MHz, DMSO-d6) δ 10.12 (s, 1H), 8.21-8.08 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07998993B2
Source datasetuspto-grants-2011_08
ORD IDord-d078c473650c43609bc53e5aa2d48076
Source noteuspto-grants-2011_08