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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1576477Generated: October 30, 2026

1-Chloro-2-nitrobenzene → HCID 21510668, compound

https://huagongshe.com/reaction/1576477

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloro-2-nitrobenzeneHCID 6945—
ReactantPotassium AcetateHCID 517044—
Reactant1-Methyl-7-(trifluoromethyl)-1H-1,5-benzodiazepine-2,4(3H,5H)-dioneHCID 21510678—
CatalystCopper SulfateHCID 24462—
SolventDichloromethaneHCID 6344—
ProductHCID 21510668HCID 21510668—

Reaction Steps

26 gm. (0.1 mol) of 1-methyl-7-trifluoromethyl-1,5-benzodiazepine-2,4-(3H,5H)-dione were heated with 13 gm. of potassium acetate, 1 gm. of anhydrous copper sulfate and 350 gm. of o-chloro-nitrobenzene for one hour at 150°C. The reaction solution was diluted with methylene chloride, washed with dilute ammonia, sodium hydroxide solution and water, the organic phase was dried, and the solvent evaporated in vacuo. The residue was carefully admixed with petroleum ether, whereby a precipitate was formed, which was recrystallized from methylene chloride/isopropylether. Yield: 30 gm. (80% of theory) of the compound of the formula ##SPC9##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE028972
Source datasetuspto-grants-1976_09
ORD IDord-bc6c3d95a244449783e6cfec5997427f
Source noteuspto-grants-1976_09