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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 345536Generated: October 26, 2026

Nitric Acid → 4-(Acetylamino)-2-ethoxy-5-nitrobenzoic Acid Methyl Ester

https://huagongshe.com/reaction/345536

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
ReactantEthopabateHCID 6034—
ReactantAcetic AnhydrideHCID 7918—
SolventAcetic AcidHCID 176—
Product4-(Acetylamino)-2-ethoxy-5-nitrobenzoic Acid Methyl EsterHCID 1509675047.9%

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of 118.6 parts of methyl 4-(acetylamino)-2-ethoxybenzoate, 200 parts of acetic acid and 156 parts of acetic acid anhydride was stirred and heated to 50° C. After cooling to 15° C. (ice-bath) there were added dropwise 47.1 parts of fuming nitric acid 100% using a bromine funnel: an exothermic reaction occured. The temperature was kept at about 20° C. by cooling in an ice-bath. Upon completion, the temperature was allowed to rise to 40° C. and stirring was continued at this temperature for one hour. If necessary the whole was cooled with ice-water to keep the temperature at about 40° C. When the exothermic reaction was ceased, the whole was allowed to cool for one hour and was further cooled to 0° C. The reaction mixture was poured onto ice-water while stirring. Upon stirring for one hour, the precipitated product was filtered off and dissolved in 1950 parts of dichloromethane. The solution was washed twice with 500 parts of water, dried, filtered and evaporated. The residue was crystallized overnight at room temperature from 2-propanol. The product was filtered off, washed with 2,2'-oxybispropane and dried, yielding 67.6 parts (47.9%) of methyl 4-(acetylamino)-2-ethoxy-5-nitrobenzoate; mp. 110° C. (intermediate 32).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05057525
Source datasetuspto-grants-1991_10
ORD IDord-9b11cee984ce4ac2a168a2e9712db290
Source noteuspto-grants-1991_10