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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1973044Generated: October 31, 2026

3,4-Dichloroaniline → HCID 22763481, compound

https://huagongshe.com/reaction/1973044

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-DichloroanilineHCID 7257—
ReactantPotassium HydroxideHCID 14797—
ReactantBenzenediazonium, 3,4-dichloro-, chlorideHCID 10262515—
ReactantSodium NitriteHCID 23668193—
ReactantHCID 86733168HCID 86733168—
SolventHydrochloric AcidHCID 313—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventSulfuric AcidHCID 1118—
ProductHCID 22763481HCID 22763481—

Reaction Steps

Prepare a solution of 3,4-dichlorophenyl-diazonium chloride by treating 8.2 g. of 3,4-dichloroaniline in 25 ml of concentrated hydrochloric acid with a solution of 3.5 g. of sodium nitrite in 35 ml of water at -5°. Dissolve ethyl 2-(2,4-dichlorobenzyl) acetoacetate (14.3 g.) in 100 ml of ethanol with 8.3 g. of potassium hydroxide in 8.3 ml of water and cool to -5°. Add the solution of the diazonium salt to the latter solution, keeping the temperature at 0°, and stir for 15 minutes. Extract with ether and wash the ether solution with two 75 ml portions of 5% sodium hydroxide and then with water and dry (MgSo4). Evaporate to yield the intermediate: ethyl 2,4-dichlorophenylpyruvate 3,4-dichlorophenyl hydrazone. The analytical sample is obtained from ethanol; m.p. 160°-161°. Dissolve the hydrazone (125 g.) in 700 ml of 20% ethanolic sulfuric acid and boil under reflux for 2 hours. Cool to room temperature and collect the crystalline product. Wash with 50% aqueous alcohol. Recrystallize from ethanol; m.p. 230°-231°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03996159
Source datasetuspto-grants-1976_12
ORD IDord-3aa0f7c9cca744088f10f0926847cfc8
Source noteuspto-grants-1976_12