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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 573509Generated: October 26, 2026

Nitrite → N-Nitrosodiphenylamine

https://huagongshe.com/reaction/573509

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitriteHCID 946—
ReactantDiphenylamineHCID 11487—
ProductN-NitrosodiphenylamineHCID 6838—

Reaction Steps

diphenylamine method, where diphenylamine as raw material is nitrosated using a nitrite in an organic solvent to produce N-nitrosodiphenylamine, which is rearranged to 4-nitrosodiphenylamine hydrochloride under the action of anhydrous hydrogen chloride, and then, 4-nitrosodiphenylamine hydrochloride is neutralized with a base to give 4-nitrosodiphenylamine which is finally reduced to 4-aminodiphenylamine by sodium sulfide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029603B2
Source datasetuspto-grants-2015_05
ORD IDord-298421b3925542f2b9d88c4bbe841300
Source noteuspto-grants-2015_05