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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1396313Generated: October 30, 2026

Pyridine → HCID 66744359, compound

https://huagongshe.com/reaction/1396313

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantMethyl chloroformateHCID 6586—
ReactantHexaneHCID 8058—
Reactant4-Iodo-3-nitroanilineHCID 284950—
SolventDichloromethaneHCID 6344—
ProductHCID 66744359HCID 66744359100%

Reaction Steps

To a cooled (0° C.), yellow suspension of 4-iodo-3-nitroaniline (8.46 g, 32.0 mmol) in DCM (320 mL) and pyridine (2.85 mL, 35.2 mmol) was added methyl chloroformate (2.61 mL, 33.6 mmol) dropwise. The reaction mixture turned to light yellow solution and stirring was continued for 1.5 h. After 1.5 h, the reaction mixture was diluted with DCM, washed with saturated NaHCO3 solution followed by brine. The organic layers were dried over MgSO4, filtered and concentrated to obtain a residue. The residue was then dissolved in DCM (˜100 mL), then hexane (600 mL) was added to give a yellow suspension. The above suspension was filtered and the filtered solid was rinsed with hexane and air-dried to obtain the desired product as yellow solid (10.3 g, 100%). MS (ESI) m/z: 321.3 (M−H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901115B2
Source datasetuspto-grants-2014_12
ORD IDord-1adb6ddf278947a687db273702d97c19
Source noteuspto-grants-2014_12