HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1915034Generated: October 31, 2026
4-Aminobenzoic Acid → Methyl 4-aminobenzoate
https://huagongshe.com/reaction/1915034
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Aminobenzoic Acid | HCID 978 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 4-aminobenzoate | HCID 12082 | 93% |
Reaction Steps
Into a 1000 mL 3-necked round bottom flask, was placed a solution of 4-aminobenzoic acid (20 g, 145.99 mmol) in methanol (600 mL). To the above was added H2SO4 (30 mL) dropwise with stirring. The resulting solution was stirred at reflux overnight. The reaction progress was monitored by TLC (EtOAc/PE=1:5). After completion, the volatile components were removed under reduced pressure and the residue was dissolved in 300 mL of water. Adjustment of the pH to 9 was accomplished by the addition of and aqueous sat. Na2CO3 solution. The resulting solution was extracted three times with 600 mL of EtOAc and the organic layers were combined and dried over Na2SO4. Removal of the volatile components under reduced pressure afforded the crude product methyl 4-aminobenzoate (vii) (20.4 g, 93% yield) as a yellow solid which was used directly in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08614321B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-ee007f5e6c7948ec8094fe271e29acce |
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| Source note | uspto-grants-2013_12 |
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