HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1361007Generated: October 25, 2026
P-Anisidine → 2-Hydroxy-5-[(4-methoxyphenylamino)methyl]benzoic Acid
https://huagongshe.com/reaction/1361007
Participants
| Role | Name | HCID | Charge |
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| Reactant | P-Anisidine | HCID 7732 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 5-Formylsalicylic acid | HCID 69226 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | 2-Hydroxy-5-[(4-methoxyphenylamino)methyl]benzoic Acid | HCID 57457041 | — |
Reaction Steps
p-Anisidine (1.3 g, 10.6 mmol) was dissolved in methanol (20 mL) and 5-formylsalicylic acid (1.75 g, 10.6 mmol) was added and the resulting mixture was stirred at room temperature for 16 hours. The solid formed was isolated by filtration, re-dissolved in N-methyl pyrrolidone (20 mL) and methanol (2 mL). To the mixture was added sodium cyanoborohydride (1.2 g) and the mixture was heated to 70° C. for 3 hours. To the cooled mixture was added ethyl acetate (100 mL) and the mixture was extracted with water (100 mL) and saturated aqueous ammonium chloride (100 mL). The combined aqueous phases were concentrated in vacuo and a 2 g aliquot was purified by SepPac chromatography eluting with mixtures of aetonitrile and water containing 0.1% trifluoroacetic acid to afford the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07879893B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-c72f71c63c074a2a9a6e5f80193b0f05 |
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| Source note | uspto-grants-2011_02 |
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