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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2075309Generated: November 1, 2026

1,1'-Carbonyldiimidazole → HCID 57991956, compound

https://huagongshe.com/reaction/2075309

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant3-Fluoro-4-nitrobenzoic acidHCID 230653—
ReactantThiosemicarbazideHCID 2723789—
SolventDimethylformamideHCID 6228—
ProductHCID 57991956HCID 5799195668%

Reaction Conditions

Temperature20 °C

Reaction Steps

3-Fluoro-4-nitrobenzenecarboxylic acid (8.4 g, 45 mmol) and 1,1′-carbonyldiimidazole (10 g, 64 mmol) were mixed in 100 mL DMF. The mixture was stirred at 20° C. for 1 hour. A clear yellow solution formed. To this mixture was added thiosemicarbazide (8.3 g, 91 mmol). The resulting mixture was stirred at 20° C. for 30 minutes. The reaction mixture was concentrated under vacuum to remove almost all the DMF. The remaining residue was treated with 2 N HCl with stirring until the solution reached pH 4. Upon standing, a yellow solid formed. The pure product was obtained as a yellow solid after filtering, washing with water, and drying (8.02 g, 68% yield). LCMS (API-ES) m/z (%): 259.1 (100%, M++H); 1H NMR (400 MHz, DMSO-d6) δ ppm 7.81 (s, 1H) 7.90 (d, J=8.41 Hz, 1H) 7.99 (s, 1H) 8.04 (d, J=11.93 Hz, 1H) 8.28 (t, J=8.02 Hz, 1H) 9.47 (s, 1H) 10.76 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07919504B2
Source datasetuspto-grants-2011_04
ORD IDord-eb226f951f4e49138878f63a58cd0002
Source noteuspto-grants-2011_04