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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1253254Generated: October 26, 2026

2-Methoxy-5-nitrobenzoic acid → 5-Amino-2-methoxybenzoic acid

https://huagongshe.com/reaction/1253254

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methoxy-5-nitrobenzoic acidHCID 284163—
Reactant1,4-Dioxane hydrochlorideHCID 20443148—
CatalystZincHCID 23994—
SolventAcetic AcidHCID 176—
Product5-Amino-2-methoxybenzoic acidHCID 13549244204.9%

Reaction Conditions

Temperature30 °C

Reaction Steps

Cyclobranyl ester of 2-methoxy-5-nitrobenzoic acid (25.0 g, 0.040 mole) prepared according to the procedure of Example 172 was suspended in acetic acid (1 l), and thereto 6N-HCl-dioxane (21 ml) and zinc powder (25.0 g) were added. The mixture was stirred at 30° C. for 2 hours. After the reaction, zinc powder was removed by filtration. The filtrate was concentrated under reduced pressure, and the residue was extracted with chloroform. The extracts were washed successively with water and saturated aqueous NaHCO3 solution, then dried, concentrated, and the residue was recrystallized from chloroform-ethanol (1:2, v/v), giving cyclobranyl ester of 5-amino-2-methoxybenzoic acid (13.7 g) in a 57.5% yield. m.p. 193°-195° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04748161
Source datasetuspto-grants-1988_05
ORD IDord-0346f0c4c2e240b389d578dd400785e2
Source noteuspto-grants-1988_05