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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 850450Generated: November 2, 2026

1-Bromopentane → 3-Amino-4-methoxybenzoic acid

https://huagongshe.com/reaction/850450

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BromopentaneHCID 8057—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Methoxy-3-nitrobenzoic acidHCID 66640—
SolventDimethylformamideHCID 6228—
Product3-Amino-4-methoxybenzoic acidHCID 17823140.8%

Reaction Conditions

Temperature100 °C

Reaction Steps

4Methoxy-3-nitrobenzoic acid (5 g, 25.4 mmol), DMF (30 ml), potassium carbonate (5.53 g, 40 mmol) and pentyl bromide (4 ml, 32.3 mmol) were mixed, and this solution was stirred at 100° C. for 1.5 hours. The reaction mixture was filtered to remove the inorganic salt, and DMF was evaporated under reduced pressure. Ethyl acetate (100 ml) was added to the obtained residue. The mixture was washed 3 times with saturated brine (30 ml) and dried over anhydrous magnesium sulfate. The drying agent was filtered off, and the filtrate was concentrated under reduced pressure. Ethanol (150 ml) and 10% palladium-carbon catalyst (0.5 g) were added to the obtained residue, and the mixture was stirred at room temperature for 5.5 hours in a stream of hydrogen. The palladium-carbon catalyst was filtered off, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by column chromatography (hexane/ethyl acetate=3/1) to give 3-amino -4-methoxybenzoic acid (5.98 g, 99% in 2 steps) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06017919
Source datasetuspto-grants-2000_01
ORD IDord-db485c985caa464abb148e6bfce41e58
Source noteuspto-grants-2000_01