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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 844112Generated: October 30, 2026

3-Nitrophenylboronic Acid → 5-(3-Nitro-phenyl)-1,3-dihydro-benzoimidazol-2-one

https://huagongshe.com/reaction/844112

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Nitrophenylboronic AcidHCID 1677—
Reactant5-Bromo-1,3-dihydro-2H-benzimidazol-2-oneHCID 12228060—
Product5-(3-Nitro-phenyl)-1,3-dihydro-benzoimidazol-2-oneHCID 9795031—

Reaction Steps

Prepared from 5-bromo-1,3-dihydro-benzoimidazol-2-one and 3-nitro-phenyl boronic acid in the same fashion as that of Example 5. White solid: mp 324-325° C.; 1H-NMR(DMSO-d6) δ10.8 (s, 2H), 8.4 (m, 1H), 8.15 (d, 1H, J=7.5 Hz), 8.1 (d, 1H, J=7.5 Hz), 7.7 (t, 1H, J=7.5 Hz), 7.35 (d, 1H, J=7.5 Hz), 7.3 (s, 1H), 7.05 (d, 1H, J=7.5 Hz); MS (ES) m/z 254 ([M−H]−, 100%); Anal. Calc. For C13H9N3O3: C, 61.18; H, 3.55; N, 16.46. Found: C, 60.5; H, 3.69; N, 15.53.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06380235B1
Source datasetuspto-grants-2002_04
ORD IDord-38d4e9ea31c64e398577aabf53540393
Source noteuspto-grants-2002_04