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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Methyl 5-amino-2-nitrobenzoate | HCID 11446896 | — |
| Reactant | Methyl 2-amino-5-(piperidin-1-yl)benzoate | HCID 61306566 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Nitro-5-propylamino-benzoic acid methyl ester | HCID 66637522 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08134015B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-baa5f130cf4f4c78a16743c1311d3d10 |
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| Source note | uspto-grants-2012_03 |
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