HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1663067Generated: October 29, 2026
Methyl Anthranilate → HCID 15922435, compound
https://huagongshe.com/reaction/1663067
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl Anthranilate | HCID 8635 | — |
| Reactant | 4-Fluorobenzaldehyde | HCID 68023 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 15922435 | HCID 15922435 | — |
Reaction Steps
To a stirred mixture of anthranilic acid methyl ester (5.0 g) and 4-fluorobenzaldehyde (3.55 ml) in 1,2-dichloroethane (50 ml) was added sodium triacetoxy-borohydride (10.5 g). The reaction mixture was stirred at room temperature for 15 hours. Saturated aqueous sodium bicarbonate was added. Layers were separated and the aqueous layer was extracted with 1,2-dichloroethane. The combined organic layers were washed with water and brine, dried (Na2SO4) and evaporated under reduced pressure. The residue was subjected to column chromatography on silica gel (elution with EtOAc/petroleum ether 1/9) and gave 2-(4-fluoro-benzylamino)-benzoic acid methyl ester (6.22 g). The obtained ester was converted into the title compound using general procedure 2. 13C-NMR (DMSO-d6) δ 169.9, 161.1, 150.4, 135.5, 134.3, 131.6, 128.9, 115.2, 114.5, 111.6, 110.4, 45.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08034811B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-a10537e5fa3d4cde9d4cf80047f2d2c8 |
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| Source note | uspto-grants-2011_10 |
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