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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1841861Generated: November 3, 2026

Sodium Iodide → HCID 86712466, compound

https://huagongshe.com/reaction/1841861

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
Reactant4-Methoxybenzoic AcidHCID 7478—
ReactantDibenzothiophene sulfoxideHCID 13898—
ReactantPhosphorus Pentoxide-Methanesulfonic AcidHCID 86584057—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 86712466HCID 8671246655%

Reaction Steps

Dibenzothiophene oxide (57 g, 285 mmol) and 4-methoxybenzoic acid (47.7 g, 314 mmol, 1.1 eq) were suspended in dichloromethane (400 mL) and cooled to 0° C. where Eaton's Reagent (285 mL) was added dropwise. The solution was taken off ice and stirred overnight at r.t. The reaction mixture was cooled back to 0° C. and quenched with the slow addition of water (800 mL), followed by ethyl acetate (500 mL). The precipitate was filtered off and the layers separated. The aqueous layer was extracted with ethyl acetate (2×500 mL) and the combined organic layers were washed with water (500 mL). Sodium iodide (341.6 g, 2.28 mol, 4 eq) in water (500 mL) was slowly poured onto the combined aqueous layers. Additional water was slowly added until precipitation of a viscous oil stopped. The crude oil was recrystallized from acetone afford the title compound (72.0 g, 55%) as a white solid. 1H NMR (300 MHz, (d-DMSO) δ: 12.0-13.0 (brs, 1H), 8.54 (d, J=7.8 Hz, 2H), 8.35 (d, J=8.1 Hz, 2H), 8.21 (dd, J=8.7, 2.1 Hz, 1H), 7.99 (t, J=7.8 Hz, 2H), 7.79 (t, J=7.8 Hz, 2H), 7.51 (d, J=8.7 Hz, 1H), 7.44 (d, J=2.1 Hz, 1H), 4.08 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08945814B2
Source datasetuspto-grants-2015_02
ORD IDord-4bd13ddb58424a6caab841109a7d001e
Source noteuspto-grants-2015_02