HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 891263Generated: October 30, 2026
Acetic Acid → Benzoic acid, 2-[(4-pyridinylmethyl)amino]-, methyl ester
https://huagongshe.com/reaction/891263
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Methyl Anthranilate | HCID 8635 | — |
| Reactant | 4-Pyridinecarboxaldehyde | HCID 13389 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Benzoic acid, 2-[(4-pyridinylmethyl)amino]-, methyl ester | HCID 10879301 | — |
Reaction Steps
3 mL Acetic acid and 8.6 g 4-pyridinecarbaldehyde are added to a solution of 7.5 g methyl anthranilate in 300 mL methanol. The mixture is stirred for 12 hours under nitrogen atmosphere at room temperature. 5.7 g Sodium cyanotrihydridoborate (85%) is added and the mixture is stirred for 3 hours at room temperature. Additional 1.14 g sodium cyanotrihydridoborate (85%) is added and the mixture is stirred for 12 hours at room temperature. The solvent is evaporated and the residue dissolved in ethyl acetate and washed with saturated NaHCO3 solution and saturated sodium chloride solution. The organic extract is concentrated and purified with hexane/ethyl acetate (1:1) on silica gel to yield methyl N-(4-pyridylmethyl)-anthranilate with m.p. 86° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07002022B2 |
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| Source dataset | uspto-grants-2006_02 |
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| ORD ID | ord-5179a70e82af4e4eb9a563e0357d2241 |
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| Source note | uspto-grants-2006_02 |
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