Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1094982Generated: November 1, 2026

Sulfuric Acid → 2-Nitro-5-propylamino-benzoic acid methyl ester

https://huagongshe.com/reaction/1094982

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantPiperidineHCID 8082—
ReactantSodium borohydrideHCID 4311764—
ReactantMethyl 5-amino-2-nitrobenzoateHCID 11446896—
ReactantMethyl 2-amino-5-(piperidin-1-yl)benzoateHCID 61306566—
SolventTetrahydrofuranHCID 8028—
Product2-Nitro-5-propylamino-benzoic acid methyl esterHCID 66637522—

Reaction Conditions

Temperature0 °C

Reaction Steps

5-Amino-2-nitro-benzoic acid methyl ester (compound A′) (800 mg) was dissolved in dry THF (15 ml). Propionaldehyde (compound D) (870 μl) dissolved in a mixed liquid composed of 3 M sulfuric acid (4 ml) and THF (1 ml) was added to the solution at room temperature. Subsequently, sodium borohydride (231 mg) was added thereto at 0° C., and the mixture was stirred at room temperature for 3 hr. Thereafter, distilled water was added thereto, and the mixture was subjected to separatory extraction with chloroform. The organic layer was washed with saturated brine, was dried over sodium sulfate and was then concentrated. The residue was purified by column chromatography using a hexane-acetone system to give 2-nitro-5-propylamino-benzoic acid methyl ester as a useful intermediate (608 mg, yield 63%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08134015B2
Source datasetuspto-grants-2012_03
ORD IDord-baa5f130cf4f4c78a16743c1311d3d10
Source noteuspto-grants-2012_03