HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 349501Generated: October 26, 2026
p-Toluenesulfonic acid → HCID 178498286, compound
https://huagongshe.com/reaction/349501
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 4-Nitrobenzonitrile | HCID 12090 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Methyl 3-Amino-4-methoxybenzoate | HCID 2734814 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 178498286 | HCID 178498286 | 52% |
Reaction Steps
Anhydrous p-toluenesulfonic acid (6.30 g, 33.1 mmol) was added to 50 ml of benzene and the resulting mixture was refluxed while removing water using a dean-stock trap. Added thereto were 3-amino-4-methoxy benzoic acid methyl ester (3 g, 16.6 mmol) obtained in step 1 of Preparation Example 1 and 4-nitrobenzonitrile (2.94 g, 19.9 mol), followed by stirring at 160° C. for 8 hours. The resulting solution was cooled to room temperature, the reaction was stopped by adding NaHCO3 thereto, extracted with ethyl acetate, the extract was dried over MgSO4 and concentrated under a reduced pressure. The resulting residue was purified by silica gel column chromatography to obtain the title compound (2.83 g, 8.59 mmol) in a yield of 52%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07179832B2 |
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| Source dataset | uspto-grants-2007_02 |
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| ORD ID | ord-f8eccf94540f43b9aff3eaedff7b2137 |
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| Source note | uspto-grants-2007_02 |
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