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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 70061Generated: October 27, 2026

Sodium Bicarbonate → HCID 178492503, compound

https://huagongshe.com/reaction/70061

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant(2-(4-Chlorophenyl)-1-(phenylsulfonyl)-1H-imidazol-4-yl)(3,4,5-trimethoxyphenyl)methanoneHCID 49788802—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178492503HCID 17849250380%

Reaction Steps

To a solution of (2-(4-chlorophenyl)-1-(phenylsulfonyl)-1H-imidazol-4-yl)(3,4,5-trimethoxyphenyl)methanone (11fa) (2.0 mmol) in THF (20.0 mL) was added 1.0 M tetrabutyl ammonium fluoride (4.0 mmol) and stirred overnight. The reaction mixture was diluted by 50 mL of saturated NaHCO3 solution (aqueous) and extracted by ethyl acetate (100 mL). The organic layer was dried over magnesium sulfate and concentrated. The residue was purified by flash column chromatography (hexane:ethyl acetate 3:1) or recrystallized from water and methanol to give a white solid. Yield: 80-95%. Yield: 36.9%; mp 193-195° C. 1H NMR (500 MHz, CDCl3) δ 10.75 (br, 1H), 7.96 (d, J=8.5 Hz, 2H), 7.83 (s, 1H), 7.47 (d, J=9.0 Hz, 2H), 7.23 (s, 2H), 3.97 (s, 3H), 3.94 (s, 6H), 2.43 (s, 3H). MS (ESI): calculated for C19H17ClN2O4, 372.1. found 395.1 [M+Na], 370.9 [M−H]−. HPLC Gradient: Solvent A (water) and Solvent B (methanol): 0-15 min 40-100% B (linear gradient), 15-25 min 100% B: tR 16.36 min, purity>99%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822513B2
Source datasetuspto-grants-2014_09
ORD IDord-09d04c0b972d4c9bb3f5eeaad4e4ba85
Source noteuspto-grants-2014_09