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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1007094Generated: October 31, 2026

1,1'-Carbonyldiimidazole → HCID 10220713, compound

https://huagongshe.com/reaction/1007094

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantHCID 9794589HCID 9794589—
SolventTetrahydrofuranHCID 8028—
ProductHCID 10220713HCID 1022071374.2%

Reaction Steps

A solution of 4-amino-3′-nitro-biphenyl-3-ol (0.115 g, 0.5 mmol) in dry THF (2.5 mL) was treated with a solution of 1,1′-carbonyldiimidazole (0.098 g, 0.6 mmol) in dry THF (2.5 mL). The reaction mixture was stirred at room temperature under a blanket of nitrogen for 6 hours. A precipitate formed, was collected and washed with methylene chloride (50 mL) to give 6-(3-nitro-phenyl)-3H-benzooxazol-2-one (0.095 g, 74%) as a white solid: mp 280-281° C.; 1H-NMR (DMSO-d6) δ 11.7 (s, 1H), 8.43 (t, 1H, J=1.15 Hz), 8.2-8.13 (nm, 21), 7.79-7.72 (m, 2H), 7.59 (dd, 1H, J=8.08, 2.31 Hz), 7.21 (d, 1H, J=8.08 Hz), MS (ES) m/z 255([M−H]−, 100%); Anal. Calc. For C13H8N2O4: C, 60.94, H, 3.15, N, 10.93. Found: C, 59.95, H, 3.17 N, 10.77.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06794373B2
Source datasetuspto-grants-2004_09
ORD IDord-ec81a77cfffa4e9cafb51c8c3e163954
Source noteuspto-grants-2004_09