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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 989182Generated: October 30, 2026

Water → (3-Aminophenyl)-3-pyridinylmethanone

https://huagongshe.com/reaction/989182

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantStannous ChlorideHCID 24479—
ReactantHCID 12930027HCID 12930027—
SolventHydrochloric AcidHCID 313—
SolventEthanolHCID 702—
Product(3-Aminophenyl)-3-pyridinylmethanoneHCID 1293002895.9%

Reaction Conditions

Temperature50 °C

Reaction Steps

3-(3-Nitrobenzoyl)pyridine (1.55 g, 0.006 mole) was suspended in ethanol (35 ml) and treated portionwise with a solution of tin (II) chloride (4.56, 0.024 mmole) in conc. HCl (7 ml). The reaction mixture was stirred at 50° C. for 2 hours. After allowing to cool to room temperature, water (50 ml) was added and the mixture basified with 10% aqueous sodium hydroxide, extracted into ethyl acetate, dried (Na2SO4) and evaporated in vacuo to afford the title compound (1.14 g, 85%) as a pale oil

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06638953B2
Source datasetuspto-grants-2003_10
ORD IDord-7a364e5f16d14a0c8dbc3abd65de2545
Source noteuspto-grants-2003_10