Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1447102Generated: October 26, 2026

Hydrochloric Acid → Benzenediazonium, 2-nitro-, chloride (1:1)

https://huagongshe.com/reaction/1447102

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-NitroanilineHCID 6946—
ReactantSodium HydroxideHCID 14798—
Reactant2,4-DicumylphenolHCID 76013—
ReactantSodium NitriteHCID 23668193—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductBenzenediazonium, 2-nitro-, chloride (1:1)HCID 148932—

Reaction Conditions

Temperature2 °C

Reaction Steps

Using the general procedure of Example 4, 13.6 grams (0.34 mole) of sodium hydroxide pellets were dissolved in 145 ml of methanol followed by the addition of 16.5 grams (0.05 mole) of 2,4-di-(α,α-dimethylbenzyl)phenol and an additional 20 ml of methanol. The resulting solution was cooled to 2° C. Meanwhile a solution of o-nitrobenzenediazonium chloride was prepared by diazotizing a mixture of 8.3 grams (0.06 mole) of o-nitroaniline and 17.3 grams of concentrated hydrochloric acid and 6 ml of water with a solution of 4.3 grams of sodium nitrite in 8 ml of water. The diazonium solution was added gradually to the alkaline solution over a two-hour period at 2° C. The resulting deep purple reaction mixture was stirred for 30 minutes at 2° C., and then acidified with 20 ml of glacial acetic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04315848
Source datasetuspto-grants-1982_02
ORD IDord-991ecd37ab57498a868edbdfaea3783f
Source noteuspto-grants-1982_02