HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1807260Generated: October 31, 2026
p-Toluenesulfonic acid monohydrate → Methyl 4-cyano-2-methoxybenzoate
https://huagongshe.com/reaction/1807260
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | 4-Cyano-2-methoxybenzoic acid | HCID 15166004 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 4-cyano-2-methoxybenzoate | HCID 57426183 | 367.8% |
Reaction Steps
A solution of 4-cyano-2-methoxy benzoic acid (1.0 g, 5.65 mmol, Biogene) in methanol was reacted with p-toluenesulfonic acid monohydrate (285.6 mg, 1.479 mmol) and heated to reflux for 16 hrs. The solvent was removed and the reaction residue was extracted with EtOAc, and washed with saturated sodium carbonate, water, and saturated NaCl, and dried over Na2SO4 to give 4-Cyano-2-methoxy-benzoic acid methyl ester (1.04 g, 96%). This ester (1.01 g, 5.28 mmol) in methanol (50 mL) was reacted with Raney Ni (3 spatula tips full, exact amount unknown, Aldrich) under 50 psi H2 in a Parr apparatus for 16 hrs. After filtering through Celite and concentrating, the crude mixture was purified by silica gel chromatography using methanol and methylene chloride to give 4-aminomethyl-2-methoxy-benzoic acid methyl ester (385.7 mg, 37%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08354444B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-584a2a7083af4124b3742acbab614677 |
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| Source note | uspto-grants-2013_01 |
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