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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2182401Generated: October 31, 2026

Nitric Acid → N-(4-ethyl-2-nitrophenyl)acetamide

https://huagongshe.com/reaction/2182401

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
ReactantN-(4-Ethylphenyl)acetamideHCID 72893—
SolventAcetic AcidHCID 176—
SolventAcetic AnhydrideHCID 7918—
ProductN-(4-ethyl-2-nitrophenyl)acetamideHCID 15919553—

Reaction Conditions

Temperature0 °C

Reaction Steps

A stirred solution of 4-ethyl-N-acetyl-aniline [3 g, Reference Example 33(a)] in acetic anhydride (8 mL) and acetic acid (4 mL), at −5° C., was treated dropwise with a mixture of acetic acid (1.75 mL) and concentrated nitric acid (1.22 mL). The mixture was warmed to 0° C., then stirred at 0° C. for 2 hours and then poured onto water. This mixture was evaporated and the resulting oil was partitioned between ethyl acetate and water. The organic layer was dried over magnesium sulfate and then evaporated. The residual oil was subjected to flash column chromatography on silica eluting with a mixture of ethyl acetate and petroleum ether (2:5) to give 4-ethyl-2-nitro-N-acetyl-aniline (1.4 g) as an orange solid. LC-MS (METHOD B): RT=2.95 minutes; 209.2 (M+H)+. (b) 4-Ethyl-5-methyl-2-nitro-N-acetyl-aniline

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06897208B2
Source datasetuspto-grants-2005_05
ORD IDord-ef538837378842ff8f445f1b32dd9dab
Source noteuspto-grants-2005_05