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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 572459Generated: November 1, 2026

Sodium Bicarbonate → HCID 178492502, compound

https://huagongshe.com/reaction/572459

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant(1-(phenylsulfonyl)-2-(p-tolyl)-1H-imidazol-4-yl)(3,4,5-trimethoxyphenyl)methanoneHCID 49788724—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178492502HCID 17849250288.5%

Reaction Steps

To a solution of (1-(phenylsulfonyl)-2-(p-tolyl)-1H-imidazol-4-yl)(3,4,5-trimethoxyphenyl)methanone (11da, 492 mg, 1.0 mmol) in THF (15.0 mL) was added 1.0 M tetrabutyl ammonium fluoride (2.0 mL, 2.0 mmol) and stirred overnight. The reaction mixture was diluted by 30 mL of saturated NaHCO3 solution (aqueous) and extracted by ethyl acetate (80 mL). The organic layer was dried over magnesium sulfate and concentrated. The residue was recrystallized from water and methanol to give a white solid of 12da (2-(p-tolyl)-1H-imidazol-4-yl)(3,4,5-trimethoxyphenyl)methanone). Yield: 88.5%. mp 201-203° C. 1H NMR (500 MHz, CDCl3) δ 10.40 (br, 1H), 7.88 (d, J=8.0 Hz, 2H), 7.82 (s, 1H), 7.31 (d, J=8.0 Hz, 2H), 7.24 (s, 2H), 3.96 (s, 3H), 3.94 (s, 6H), 2.43 (s, 3H). MS (ESI): calculated for C20H20N2O4, 352.10. found 375.2 [M+Na]+. HPLC2: tR 15.45 min, purity 97.4%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029408B2
Source datasetuspto-grants-2015_05
ORD IDord-7edb7b0d529e4bcfb98f652829966d3b
Source noteuspto-grants-2015_05