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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 52650Generated: October 26, 2026

Nitric Acid → N-(4-fluoro-2-methyl-6-nitrophenyl)acetamide

https://huagongshe.com/reaction/52650

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
ReactantO-ToluidineHCID 7242—
ReactantAcetic AnhydrideHCID 7918—
ReactantAcetyl nitrateHCID 11557—
Reactant4-Fluoro-2-methylanilineHCID 67982—
ProductN-(4-fluoro-2-methyl-6-nitrophenyl)acetamideHCID 54330341—

Reaction Conditions

Temperature7 °C

Reaction Steps

Stirred acetic anhydride, 300 mL, was cooled to about 7° C., and 25.1 grams (0.20 mole) of 4-fluoro-2-methylaniline was added dropwise during a 30 minute period. Upon completion of addition, the reaction mixture was stirred at about 10° C. for an additional 15 minutes. In a separate reaction vessel, acetyl nitrate was prepared by the dropwise addition of 14.9 mL of 90% nitric acid to 30 mL of stirred, cold (0°-15° C.) acetic anhydride during a 15 minute period. The so-prepared acetyl nitrate was cooled to about -5° C., placed in a dropping funnel, and added dropwise during a 30 minute period to the 2-methylaniline solution. Upon completion of addition, the reaction mixture was stirred an additional 5 hours. After this time the reaction mixture was poured into 400 grams of ice. The resultant solid was collected by filtration, washed with water, and dried at 60° C. under vacuum, yielding 23.0 grams of 5-fluoro-2-methylcarbonylamino-3-methylnitrobenzene, mp 167°-172° C. The NMR spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05616718
Source datasetuspto-grants-1997_04
ORD IDord-e3c956dc6aac4315bf1090e7f781f7ff
Source noteuspto-grants-1997_04