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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 436543Generated: October 26, 2026

2-Methyl-4-nitroaniline → Acetamide, N-(2-methyl-4-nitrophenyl)-

https://huagongshe.com/reaction/436543

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methyl-4-nitroanilineHCID 7441—
ReactantAcetic AnhydrideHCID 7918—
SolventAcetic AcidHCID 176—
SolventTetrahydrofuranHCID 8028—
ProductAcetamide, N-(2-methyl-4-nitrophenyl)-HCID 75936—

Reaction Steps

349.6g (2.3 moles) of 4-amino-3-methyl-nitrobenzene were dissolved in 500g of tetrahydrofuran, 500g of acetic acid were added thereto, and 500g (3.5 moles) of acetic anhydride were added dropwise while stirring and heating at 70° to 80° C, and, after the completion of the acetic acid addition, the entire reaction system was reacted for 1 hour under reflux and then was allowed to cool whereby crystals were formed. The crystals were separated, filtered out and then dried.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04009205
Source datasetuspto-grants-1977_02
ORD IDord-e8f415aedd1a4dbf882e872f0137502f
Source noteuspto-grants-1977_02