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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1966283Generated: October 30, 2026

Ethyl Acetate → Methyl 5-amino-2-bromobenzoate

https://huagongshe.com/reaction/1966283

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium HydroxideHCID 14798—
ReactantStannous ChlorideHCID 24479—
ReactantMethyl 2-Bromo-5-nitrobenzoateHCID 245494—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductMethyl 5-amino-2-bromobenzoateHCID 24549594%

Reaction Steps

Methyl 2-Bromo-5-nitrobenzoate (25.3 g, 97.3 mmol) was dissolved in anhydrous methanol (50 mL), and tin (II) chloride (93.3 g, 487 mmol) was added thereto, and then the reaction mixture was refluxed for 2 hours. After cooling down, ethyl acetate (500 mL) and water (100 mL) were added thereto, and the mixture was neutralized with 4N aqueous NaOH solution, and then it was filtered on celite. The filtrate was concentrated under reduced pressure, and ethyl acetate (200 mL) was added thereto, and then it was washed with saturated NaHCO3 solution (200 mL, twice), water (200 mL) and saturated brine (200 mL) successively. The organic layer was dried over anhydrous magnesium sulfate and the solvent was removed under reduced pressure to give the titled reference compound (21.0 g) as a yellow oil. (Yield 94%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08420635B2
Source datasetuspto-grants-2013_04
ORD IDord-5ee4983d5f4d40caaa7a597d4b0dc862
Source noteuspto-grants-2013_04