HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1672571Generated: October 30, 2026
Water → 4-(Pentafluoro-lambda6-sulfanyl)benzaldehyde
https://huagongshe.com/reaction/1672571
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Hexamethylphosphoramide | HCID 12679 | — |
| Reactant | 4-Iodophenylsulfur Pentafluoride | HCID 2779199 | — |
| Reactant | HCID 178418416 | HCID 178418416 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-(Pentafluoro-lambda6-sulfanyl)benzaldehyde | HCID 2779207 | 86% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07998993B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-d078c473650c43609bc53e5aa2d48076 |
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| Source note | uspto-grants-2011_08 |
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