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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1940732Generated: November 1, 2026

1,2-Dichlorobenzene → HCID 21463639, compound

https://huagongshe.com/reaction/1940732

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichlorobenzeneHCID 7239—
ReactantHCID 21463675HCID 21463675—
ReactantN-methyl-N-(p-toluenesulfonyl)-2-chloro-6-fluorobenzohydrazonoyl chlorideHCID 54347086—
CatalystIron chloride (FeCl3)HCID 24380—
SolventChloroformHCID 6212—
ProductHCID 21463639HCID 2146363940.8%

Reaction Conditions

Temperature140 °C

Reaction Steps

A mixture of N-methyl-N-(p-toluenesulfonyl)-2-chloro-6-fluorobenzohydrazonoyl chloride (1.00 g), 3,5-dichloro-4-(3-chloro-5-trifluoromethylpyridine-2-yloxy)benzonitrile (1.00 g), anhydrous iron (III) chloride (0.50 g) and o-dichlorobenzene (5 ml) is stirred at an oil bath temperature of 140° C. for 30 minutes. After cooling, it is dissolved in chloroform (100 ml) and washed with dilute hydrochloric acid, dilute aqueous solution of sodium hydroxide and saline. Then, it is dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The concentrate is purified by silica gel column chromatography using mixed solvent of hexane-ethyl acetate as eluent to give 0.60 g of desired compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05700824
Source datasetuspto-grants-1997_12
ORD IDord-191a04b5b48447eda72df797f0c9cd60
Source noteuspto-grants-1997_12