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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 340617Generated: October 29, 2026

Stannous Chloride → Methyl 3-amino-5-(5-methylpyridin-2-yl)benzoate

https://huagongshe.com/reaction/340617

Reaction equation

Participants

RoleNameHCIDCharge
ReactantStannous ChlorideHCID 24479—
Reactant3-(5-Methyl-pyridin-2-yl)-5-nitro-benzoic acid methyl esterHCID 57851658—
SolventEthylacetate methanolHCID 21584119—
ProductMethyl 3-amino-5-(5-methylpyridin-2-yl)benzoateHCID 5785101890%

Reaction Steps

To a solution of 3-(5-methyl-pyridin-2-yl)-5-nitro-benzoic acid methyl ester (4 g, 14.7 mmol) in methanol/ethyl acetate was added SnCl2 (11.15 g, 58.8 mmol) at room temperature. The reaction mixture was refluxed for 3 hours and then cooled. Solvent was removed under reduced pressure and the residue was dissolved in H2O and basified by addition of Na2CO3 to pH=9. The mixture was extracted with CH2Cl2, and the organic phase was washed with water, brine, and dried over Na2SO4. The solvent was removed under reduced pressure to give 3-amino-5-(5-methyl-pyridin-2-yl)-benzoic acid methyl ester (3.2 g, 90%) as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895589B2
Source datasetuspto-grants-2014_11
ORD IDord-b1c00257a5e946ecb6aaef55ed3d1133
Source noteuspto-grants-2014_11